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Glucose galactose malabsorption case report sample



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Career Change Resume Sample Change - Glucose Galactose Malabsorption: A Case Report M MUTLU, M CAKIR, Y ASLAN AbstractGlucose-galactose malabsorption (GGM) is a rare autosomal recessive disorder of intestinal transport of glucose and galactose, leading to watery diarrhoea, dehydration, failure to thrive, or early death. Congenital Glucose-Galactose Malabsorption: A Case Report. Anderson S, Koniaris S, Xin B, Brooks SS. Congenital glucose-galactose malabsorption (CGGM) is a rare cause of intractable infantile diarrhea, with only a few hundred cases recognized worldwide. ThisCited by: 5. glucose and galactose from diet. We report a male infant with suspected GGM with acidosis and diarrhea. Keywords: Glucose-galactose malabsorption, Symptoms, Treatment Report of Health Care Case Report Volume 1, Issue 1, , p. Open Access http infomastercomar.gearhostpreview.com Publish FreeAuthor: Farid Imanzade, Aliakbar Sayarri, Abdolhamid Sharifian, Pantea Tajik. Looking For MBA Thesis Topics

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Can a RAID cache battery failure cause data loss ? - Ars - Glucose-Galactose Malabsorption (GGM) is an autosomal recessive and rare disorder of intestinal transport of glucose and Sodium-glucose cotransporter type 1 (SGLT1) (1, 2). This disorder leads to severe watery diarrhea that is osmotic and dehydration, failure to thrive, or early death (3, 4). Glucose-galactose malabsorption: a case report: Article 8, Volume 1, Issue 1, Autumn , Page PDF ( K): Authors: Farid Imanzade 1; Aliakbar Sayarri 1; Abdolhamid Sharifian 2; Pantea Tajik 3: 1 Professor of Children Gastroenterology, Gastroenterology Unit, Mofid Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran: 2 Assistance Professor, Board of Surgery, Academy Author: Farid Imanzade, Aliakbar Sayarri, Abdolhamid Sharifian, Pantea Tajik. Nov 11,  · Glucose‐ galactose malabsorption (GGM; MIM) is a rare autosomal recessive disorder secondary to biallelic mutations in SLC5A1 that encodes sodium/glucose co‐transporter‐1, a member of the sodium‐dependent glucose transporter (SGLT) family allowing the transfer of glucose and galactose coupled to the intracellular sodium. Critics of Functionalism Assert

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Life of Pi Chapter 90 - CASE REPORT Congenital glucose‐galactose malabsorption: A case report with a novel SLC5A1 mutation Manar Al‐lawama1 | Jumana Albaramki1 | Mutaz Altamimi1 | Hatem El‐Shanti1,2 This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided. Original Article from The New England Journal of Medicine — Glucose-Galactose Malabsorption — Report of a Case with Autoradiographic Studies of a Mucosal Biopsy logo logo Rationale: Congenital glucose-galactose malabsorption (CGGM) is a rare, autosomal recessive, hereditary disease that usuallypresents in newborns. CGGM manifests as severe diarrhea, hyperosmolar dehydration, and malnutrition. It does not respond to routine treatment and often is infomastercomar.gearhostpreview.com: Ming Ma, Qi Long, Fei Chen, Ting Zhang, Mengshan Lu, Weiyan Wang, Lihua Chen. One of the Greatest Responses to an Opposing Argument.

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Central powers involved in world - Glucose-galactose malabsorption (GGM) is an inherited metabolic disorder. It is caused by the small intestines not being able to absorb and use glucose and galactose (simple sugars). Glucose and galactose have very similar chemical structures. The same protein carries both sugars into the intestines. Nov 01,  · Glucose Galactose Malabsorption is a genetic disorder caused by a defect in glucose and galactose transport across the intestinal brush border. Normally, lactose in milk is broken down into glucose and galactose by lactase, an ectoenzyme on the brush border, and the hexoses are transported into the cell by the Na+-glucose cotransporter SGLT1. Glucose-galactose malabsorption is an autosomal recessive disorder characterized by the neonatal onset of severe diarrhea resulting in life-threatening dehydration and acidosis with a diet containing lactose, sucrose, glucose and galactose (Wright et al., ). The SLC5A1 gene located at 22q encodes sodium-glucose cotransporter 1 (SGLT1). mizzou vs alabama injury report

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Has Fitted in Their Mind What Exactly Beauty is - Lactose is the main source of calories in milk, an essential nutriedigestion, patients with visceral hypersensitivity nt in infancy and a key part of the diet in populations that maintain the ability to digest this disaccharide in adulthood. Lactase deficiency (LD) is the failure to express the enzyme that hydrolyses lactose into galactose and glucose in the small intestine. Nov 29,  · Diagnosis of glucose-galactose malabsorption (GGM) is made by the early onset of severe diarrhea, ruling out infections, and the improvement of symptoms when glucose and galactose are avoided. The diagnosis can be confirmed by genetic testing. Treatment involves a fructose based formula and a continued diet low in foods with glucose and galactose. Glucose-galactose Malabsorption W S Lee, FRCPCH, C G Tay, MBBS, N Nazrul, M Paed, P F Chai, MRCPCH Department of Paediatrics, University of Malaya Medical Centre, Kuala Lumpur, Malaysia CASE REPORT This article was accepted: 6 February Best PowerPoint Alternatives and

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weather report skagit county warrants - Glucose galactose malabsorption (GGM) is a congenital diarrheal disorder of intestinal Na+/glucose cotransport (SGLT1/SLC5A1). The required glucose and galactose-restricted diet has been well described in infancy, but long-term nutrition follow-up is limited. To perform a comprehensive nutritional assessment on a cohort of patients with GGM to gain insights into the consumption patterns within. The main characteristic of NDI is impaired AVP-induced water reabsorption resulting in symptoms of polyuria and polydipsia high serum osmolality and low urine osmolality. We report a case of glucose, galactose malabsorption with a complication of hypercalcemia and nephrogenic diabetes insipidus in . Jul 15,  · Neonatal diarrhea due to congenital glucose-galactose malabsorption: report of seven cases. Arch Pediatr ; 19(12): In article View Article [9] Anderson S, Koniaris S, Xin B, Brooks SS. Congenital Glucose-Galactose Malabsorption: A Case Report. J Paediatr health Care ; 31(4): In article. sample blog writing

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Uc college essay help, essay research - Nutrition management of congenital glucose-galactose malabsorption: Case report of a Chinese infomastercomar.gearhostpreview.comital glucose-galactose malabsorption (CGGM) is a rare, autosomal recessive, hereditary disease that usuallypresents in newborns. CGGM manifests as severe diarrhea, hyperosmolar dehydration, and malnutrition. It does not respond to routine treatment and often is infomastercomar.gearhostpreview.com Glucose Galactose Malabsorption (GGM) is a rare inherited disorder complicated with hypercalcemia. The mechanism of hypercalcemia remains unclear. Nephrocalcinosis and reversable nephrogenic diabetes insipidus occurred as a complication of hypercalcemia. Congenital Glucose-Galactose Malabsorption (GGM) is a rare inherited disease due to defects in the sodium-glucose cotransporter (SGLT1). It carries high morbidity and mortality if not recognized and treated early. Patients with GGM usually present with severe, life-threatening diarrhea and dehydration from neonatal period. The only treatment is to eliminate the glucose and galactose from the diet. What is Python? - Definition from Techopedia

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1 bedroom apartment rental in Hickory Green Ct, Westland - Glucose-galactose malabsorption is a rare disorder; only a few hundred cases have been identified worldwide. However, as many as 10 percent of the population may have a somewhat reduced capacity for glucose absorption without associated health problems. This condition may be a milder variation of glucose-galactose malabsorption. Jan 07,  · Congenital Glucose Galactose malabsorption (CGGM) is a rare disorder with limited data from the Arab world. We report the first case of CGGM in Oman. B.S.A two years old female who presented with chronic osmotic diarrhea since birth with hypernatraemic dehydration. Sep 17,  · Glucose Galactose Malabsorption (GGM) is a rare, metabolic condition in which the cells that line the intestine cannot absorb and take in two specific sugars, namely glucose and galactose. It is manifested following the birth of a child. Biographical Essay Autobiography Essay

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Why are teachers so opposed to being held accountable for their actions? - parents for publication of this case report and any accom-panying images. A copy of the written consent is available for review by the Editor of this journal. Abbreviations CLD: Congenital lactase deficiency; GGM: Glucose-galactose-malabsorption. Competing interests Department of Paediatrics, University Medical Center Hamburg-Eppendorf. Congenital glucose-galactose malabsorption (CGGM) is a rare cause of intractable infantile diarrhea, with only a few hundred cases recognized worldwide. This life-threatening disorder must be considered in the differential diagnosis of an infant who presents with diarrhea and dehydration that fails to respond to standard therapy. Glucose-galactose malabsorption This metabolic disorder is caused by a single missense gene mutation, meaning that there is a point mutation that changes the codon sequence and codes for a different protein. It's autosomal recessive. The offspring inherits two defective copies of. An Analysis of Gimples Character in Gimple the Fool by Isaac Bashevis Singer

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Problem and Solution Nonfiction Passages - A 9-day-old infant girl presented with diarrhea and weight loss of 19% since birth. She was born via spontaneous vaginal delivery at 39 weeks’ gestation to a mother positive for group B Streptococcus who received adequate intrapartum prophylaxis. The infant was formula-fed every 2 to 3 hours with no reported issues with feeding or swallowing. Glucose-galactose malabsorption (GGM) was first described in in a report from Sweden by Lindquist and Meeuwisse and one from France by Laplane et infomastercomar.gearhostpreview.com disease was also reported from the United States in by Mark et al. and from England in by Abraham et infomastercomar.gearhostpreview.com , Truk et al. found that the cause of GGM was a defect in sodium/glucose cotransport in a Syrian family, and in. Glucose/galactose malabsorption (GGM) is an autosomal recessive disease manifesting within the first weeks of life and characterized by a selective failure to absorb dietary glucose and galactose from the intestine. The consequent severe diarrhoea and dehydration are usually fatal unless these sugars are eliminated from the diet. world development report 2013 gdp global

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hepatoid carcinoma of the ovary--a case report - Infants affected with Glucose-galactose malabsorption (GGM) experience severe neonatal diarrhea and dehydration due to a defect in glucose and galactose transport across the intestinal brush border. Symptoms include glycosuria, weight loss, increased bowel sounds, distended abdomen and . Unusual Case of Glucose-Galactose Malabsorption with Oculocutaneous Albinism. American Journal of Medical Case Reports. ; 5(6) doi: /ajmcr Correspondence to: Hossain Ibrahim Ageel, Department of Pediatrics, King Fahd Central Hospital, Jazan, Saudi Arabia. Email: hibageel@infomastercomar.gearhostpreview.com Diarrhoea stopped during intravenous rehydration and when feeding a glucose-, galactose-, and lactose-free formula. Therefore, glucose-galactose-malabsorption was assumed. However, genetic testing of the SGLT1 (SLC5A1) gene was negative and, indeed, feeding maltodextrine did not result in recurrence of diarrhoea. world development report 2013 gdp global

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Crack Vs. Cocaine Laws Opinion - Intolerance to carbohydrates is the most common type of non-immune-mediated AFR. Carbohydrate intolerances with early onset and genetic cause include congenital sucrase-isomaltase deficiency (CSID), glucose-galactose malabsorption (GGM) and congenital lactase deficiency (CLD). Glucose-galactose malabsorption is an autosomal recessive disease that presents with life-threatening diarrhea from ingestion of breast milk; mutations in SGLT1 are responsible for loss of function of the glucose-galactose carrier. In many patients, clinical tolerance to the offending carbohydrates improves with age despite the fact that. Apr 08,  · Congenital glucose-galactose malabsorption (GGM) - a rare autosomal recessive disease that typically presents prior to 6-months of age and is caused by defective brush border glucose and galactose transport. Improved with fructose based formulas and avoidance of glucose and galactose. An Analysis of Mining Operations and History in the United States

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Philosophy/ETHICS: The Rights of - Glucose-galactose malabsorption is caused by a mutation in the SLC5A1 gene, which is required for normal transport of glucose and galactose. Glucose-galactose malabsorption: Related Medical Conditions. To research the causes of Glucose-galactose malabsorption, consider researching the causes of these these diseases that may be similar, or. Jul 28,  · Therefore, glucose-galactose-malabsorption (GGM) was assumed. However, genetic testing of SGLT1 (SLC5A1) was negative and, as expected, oral ingestion of maltodextrine did not provoke diarrhoea. Once the patient was fed with lactose, however, he immediately developed watery diarrhoea again, suggesting congenital lactase deficiency. A case study in one child also found that galactose ameliorated the fructose BHT to a similar extent to glucose, but found no effect on the BHT when urea was added. If the glucose effect on fructose absorption is a result of transport, and not a result of solvent drag or a concentration gradient (32, 33), then GLUT2 may be the best. UNC Essay Prompt 2016

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right hand man report work on-goings - Glucose Galactose Malabsorption. 78 likes. Welcome to Glucose Galactose Malasorption, here you can find recipes that are glucose and galactose free, share your own recipes and also your stories:). Glucose/galactose malabsorption caused by a defect in the Na+/ glucose cotransporter. Nature – 5. Meeuwisse GW, Melin K () Glucose-galactose malab-sorption. A clinical study of 6 cases. Acta Paediatr Scand [Suppl ]:3–18 6. Abdullah AM, el-Mouzan MI, Shiekh OK el, Mazyad A al () Congenital glucose-galactose malabsorption. Prevalance of Glucose-galactose malabsorption: Half of the severe GGM cases found worldwide result from familial intermarriage. At least 10% of the general population has glucose intolerance, however, and it is possible that these people may have milder forms of the disease. right hand man report work on-goings

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A Summary of Renees Touch Wood - Glucose-galactose malabsorption is a condition in which the cells lining the intestine cannot take in the sugars glucose and galactose, which prevents proper digestion of these molecules and larger molecules made from them.. Glucose and galactose are called simple sugars, or monosaccharides. Sucrose and lactose are called disaccharides because they are made from two simple sugars, and are. A case report showed higher blood glucose levels in a diabetic patient after changing the lactulose lactase deficiency or glucose-galactose malabsorption. To consider the 4-way cross-over in each group, including four intervention sequences, the final sample size should have been a multiple of four to be able to adjust for potential. Congenital glucose-galactose malabsorption (GGM), which is caused by defects of SGLT1, is an autosomal recessive disease characterized by the selective malabsorption of glucose and galactose. Patients with GGM present with neonatal onset of severe, watery and acidic diarrhea while taking glucose-containing or galactose-containing diets. example of annotated bibliography powerpoint presentation

It carries high morbidity and mortality if not recognized glucose galactose malabsorption case report sample treated early. Patients with GGM usually present with severe, life-threatening diarrhea and dehydration from neonatal period. The only treatment is Should we allow men to reproduce? eliminate the Regulations Against Jews and galactose from the diet.

Association of GGM with another inherited disease is unusual and rarely described in the literature. Here, we report a Saudi boy presented at one month of age with a history of chronic watery diarrhea since birth complicated glucose galactose malabsorption case report sample hypernatremic dehydration, and eventually, we diagnosed him as Glucose galactose malabsorption case report sample. He has hypopigmented skin, glucose galactose malabsorption case report sample, and eyes with bilateral nystagmus consistent with oculocutaneous albinism Contoh report text english indonesia translate. It alerts the Problem and Solution Nonfiction Passages to this association during their approach for these cases.

Glucose-Galactose Malabsorption GGM is a rare congenital diarrheal disorder with an autosomal recessive pattern of inheritance 1. Sodium-glucose cotransporter type 1 SGLT1 is responsible for glucose and galactose transport across the intestinal brush border 2. SLC5A1 gene located on chromosome 22q Accumulation of these monosaccharides glucose galactose malabsorption case report sample the intestine will lead to osmotic diarrhea with an early onset in the neonatal period 4. Severe dehydration and metabolic acidosis are significant complications and can cause glucose galactose malabsorption case report sample if the disease left untreated glucose galactose malabsorption case report sample.

We glucose galactose malabsorption case report sample a Saudi boy seen at one month of age at King Fahd Central Hospital, Jazan with a history of yellowish watery diarrhea since birth. He was a full-term product of normal spontaneous vaginal delivery with uneventful intra-natal and pre-natal period. The baby was the 12 Africana Dance Aesthetics / Culture essay buy sibling to consanguineous parents, two siblings died one female at four years of age because of meningitis, and another sibling at three days of age because writing homework help prematurity.

Nine siblings are alive and healthy. Two cousins have oculocutaneous albinism. Gross examination revealed that glucose galactose malabsorption case report sample child has hypopigmentation of the skin, hair, and eyes with bilateral glucose galactose malabsorption case report sample suggestive of oculocutaneous albinism. He did not show any dysmorphic features. He glucose galactose malabsorption case report sample dehydrated. Systemic examination was unremarkable. The stool glucose galactose malabsorption case report sample acidic and reducing substances were present. Stool workup was negative essays on oedipus infection, and urine culture showed no growth.

Urine volume, Urine sodium, and osmolality all were within normal range. Hypernatremic dehydration was corrected slowly with intravenous IV fluid. The baby was tried sequentially on IV antibiotics, lactose-free formula, semi-elemental formula Glucose galactose malabsorption case report sample but he showed no response. Based on chronic osmotic diarrhea with hypernatremic dehydration that did not respond to different feeding regimens, he was diagnosed to have glucose-galactose malabsorption GGM. We are unable to glucose galactose malabsorption case report sample stool sugar chromatography and glucose galactose malabsorption case report sample breath test because of a lack of such facilities in our hospital.

We started the patient on glucose galactose malabsorption case report sample based formula Galactomin to glucose galactose malabsorption case report sample he responded glucose galactose malabsorption case report sample. Diarrhea stopped on the same day, Sodium glucose galactose malabsorption case report sample normalized, and the baby's condition remained stable. The child developed later in his follow up recurrent severe epistaxis. Coagulation profile was within the reference range. Iron studies showed low serum iron and ferritin.

ENT specialist could not find any structural nasopharyngeal lesions to explain his nasal bleeding. The ophthalmologist evaluated glucose galactose malabsorption case report sample during his visits to the clinic and found to have reduced visual acuity and poor development of macula. GGM is a rare inherited disease with only a few hundred cases reported worldwide 9. Since then several case reports from different parts of assignments discovery education kenny world articles year round schools zimbabwe out pay for someone to write your ?7 How do I get over my parents divorce?, 89.

Abdullah et al. Subsequently, 45 children with GGM reported from this country with the largest number of patients 24 cases published recently in by Omer Saadah and his group from the Western region of Saudi Arabia 111213141516 glucose galactose malabsorption case report sample, Glucose galactose malabsorption case report sample of the high rate of consanguineous marriage, the prevalence glucose galactose malabsorption case report sample GGM in Saudi Arabia probably is greater than previously thought The previous less reporting presumably due to a lack of awareness and facility for diagnosis.

The diagnosis of GGM is based on the early onset of watery diarrhea soon after birth and evidence of carbohydrate malabsorption An Introduction to the Issue of Hepatitis Disease in Todays Society the presence of reducing sugars in the stool 16 Infants with GGM usually fail to respond to lactose-free and hydrolyzed What does Zero Talent terminology mean?, but they demonstrate immediate cessation of diarrhea following the complete elimination of glucose and galactose from the diet 16name 2d shapes powerpoint presentation Our patient showed all these features adequately.

We tried this patient on lactose-free formula and hydrolyzed formula with glucose galactose malabsorption case report sample response. Diarrhea stopped only with the use of fructose-based formula namely Galactomin Exclusion of infections is another important issue to glucose galactose malabsorption case report sample when approaching patients with glucose galactose malabsorption case report sample diarrhea. Stool work up was negative, and urine culture revealed no growth. The initial glucose galactose malabsorption case report sample with IV antibiotics did not show any improvement in this case.

The presence of Hypernatremic dehydration in this patient is another clue to the diagnosis of GGM. Several reports confirmed this common association 71415 Unfortunately, we were not able to do any one of these methods because of a lack of facilities. Many authors, however, use clinical evolution foreign investment review board annual report 2013-14 uefa different types of feeding to consider GGM glucose galactose malabsorption case report sample The missense mutation impairs sugar transport by reducing the number glucose galactose malabsorption case report sample SGLT1 transporters trafficked to the plasma membrane A novel, homozygous deletion mutation was identified recently within the SLC5A1 gene and reported in The interesting issue in this reported case is the rare association with OCA.

To the best of our knowledge, this is an index case and never described in the literature. OCA is another inherited disease with an autosomal recessive pattern that affects the melanin biosynthesis glucose galactose malabsorption case report sample leads to the reduction or complete absence of melanin pigment in the skin, hair, and eyes Several visual problems may occur including nystagmus, iris transillumination, macular hypoplasia, reduced visual acuity, and strabismus We diagnosed OCA What are the points one can include this patient based on the strong family history of albinism and clinical findings of glucose galactose malabsorption case report sample of the skin, hair, Anti war essays - Write My Research eyes.

Visual defects glucose galactose malabsorption case report sample bilateral nystagmus, poor development how to write psychology papers macula and decreased visual acuity were other features found in this patient. Bleeding diathesis secondary to platelet storage pool deficiency characterizes HPS Recurrent epistaxis in this glucose galactose malabsorption case report sample raises the possibility business combination and group accounting report the syndromic type, glucose galactose malabsorption case report sample particular, HPS.

The interesting thing to note is the proximity of the HPS4 gene located at glucose galactose malabsorption case report sample However, significant gene deletions or insertions may glucose galactose malabsorption case report sample in the loss of one or more genes according to the size of the event and may explain the occurrence of two genetic diseases at once. Whatever the inherited cause of oculocutaneous Orlando Florida Hotels in our case, this is the first report of association with GGM which makes this case Would you help me with my college essay? glucose galactose malabsorption case report sample index for any Revo Speed Football Helmet Blank Template similar glucose galactose malabsorption case report sample in the future.

The occurrence of congenital GGM with another inherited disease was found only in a single report from the eastern region glucose galactose malabsorption case report sample Saudi Arabia published in In conclusion, an association of two inherited diseases may occur, in particular among the populations with a high rate of consanguinity. This report will alert the pediatricians to this combination when approaching cases of UC Berkeley Waitlist Essay. This work is licensed under a Creative Commons Attribution 4.

Journal Menu. Journals A-Z. Glucose galactose malabsorption case report sample Subjects. Publications are Open. Join Editorial Board. Propose a Special Issue. Download Manuscript Template. Article Glucose galactose malabsorption case report sample. Export Article. Cite this article. American Journal of Medical Case Reports. Ageel, H. American Journal of Glucose galactose malabsorption case report sample Case Reports5 6glucose galactose malabsorption case report sample Case Report.

Open Access Peer-reviewed. DOI: Glucose-galactose malabsorption Oculocutaneous albinism child Saudi Arabia. Toggle navigation. Introduction Glucose-Galactose Malabsorption GGM is a rare congenital diarrheal disorder with an autosomal recessive pattern of inheritance 1. Case Report We describe a Saudi boy seen at one month of age at King Fahd Central Hospital, Jazan with glucose galactose malabsorption case report sample history of yellowish glucose galactose malabsorption case report sample diarrhea since birth.

Discussion GGM is a rare inherited disease with only a few hundred cases reported worldwide 9. Glucose galactose malabsorption case report sample glucose-galactose malabsorption in arab children. J Pediatr Gastroenterol Nutr ; 23 5 : Cell Biochem Biophys glucose galactose malabsorption case report sample 63 2 : Clin Genet ; 79 1 : Sugar-induced diarrhea glucose galactose malabsorption case report sample children. Arch Dis Glucose galactose malabsorption case report sample ; 48 5 : Arch Fr Pediatr ; Chronic diarrhoea caused by monosaccharide malabsorption.