Meckel-Gruber Syndrome Information Diseases Database MeckelGruber syndrome,dysencephalia splanchnocystica, Disease Database dysencephalia splanchnocystica. may cause or feature + (Follow link for list. http://www.diseasesdatabase.com/ddb31661.htm
Extractions: Meckel-Gruber Syndrome - Meckel-Gruber syndrome (MKS) (OMIM 24900) is a lethal, rare autosomal recessive condition mapped to chromosome 17. The triad of occipital encephalocele, large polycystic kidneys, and postaxial polydactyly characterizes MKS. Associated abnormalities include oral clefting, genital anomalies, CNS malformations, and fibrosis of the liver. Pulmonary hypoplasia is the leading cause of death. With the advent of ultrasonography, prenatal diagnosis is possible during the second trimester or late first ...
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The Turkish Journal Of Pediatrics syndrome (MGS) was first described by Meckel in 1822 and then in 1934 byGruber, who gave the complex name dysencephalia splanchnocystica 1. http://tjp.dergisi.org/text.php3?id=204
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Search By Disease 161 Dyschondrosteosis (DCO). 162 dysencephalia splanchnocystica. 163Dyserythropoietic anemia, congenital, type II. 164 Dyserythropoietic anemia, hempas http://www.eddnal.com/directory/disease.php?letter=D&page=11
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D Conditions And Diseases Health Interactiva Dwarfism English Health Conditions and Diseases Musculoskeletal Disorders CongenitalAnomalies Dwarfism ? dysencephalia splanchnocystica English Health http://www.interactiva.org/Dir/I/English/Health/Conditions_and_Diseases/D/
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Health Encyclopedia National Organization for Rare Disorders, Inc. Synonyms. dysencephalia splanchnocystica;Gruber Syndrome; MeckelGruber Syndrome; MES; MKS. Disorder Subdivisions http://members.kaiserpermanente.org/kpweb/healthency.do?body=nord/nord661&navtop
