Research Paper | Medicine Science | India | Volume 3 Issue 9, September 2014
Dr. Muruganantham Balagurunathan, Dr. Ramesh Samikannu, Dr. Ramanathan Ramanathan
Abstract: Dysencephalia Splanchnocystica also called as Meckel-Gruber syndrome is an autosomal recessive disorder1. It is characterized by a traid of occipital encephalocele, large polycystic kidneys, and postaxial polydactyly2. The major diagnostic criteria of MGS include at least 2 of these 3 classic manifestations, occipital encephalocele, cystic renal dysplasia, and polydactyly found in 90 %, 100 % and 83.3 % respectively 3. It is a rare syndrome with highest incidence in Gujarati Indians and Finnish population. We are reporting a case of Dysencephalia Splanchnocystica in a non Gujarati Indian from a municipal town, Sirkazhi in Nagapattinam district in Tamil Nadu, India.
Keywords: Dysencephalia Splanchnocystica, Occipital encephalomeningocele, Postaxial polydactyly
Edition: Volume 3 Issue 9, September 2014,
Pages: 2301 - 2302
How to Cite this Article?
Dr. Muruganantham Balagurunathan, Dr. Ramesh Samikannu, Dr. Ramanathan Ramanathan, "Dysencephalia Splanchnocystica", International Journal of Science and Research (IJSR), https://www.ijsr.net/get_abstract.php?paper_id=SEP14628, Volume 3 Issue 9, September 2014, 2301 - 2302
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