Meckel-Gruber Syndrome: Revision history

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12 December 2023

  • curprev 20:1220:12, 12 December 2023‎ Ai talk contribs‎ 3,487 bytes +3,487‎ Created page with "== Overview == Meckel-Gruber Syndrome (MKS) is a rare, lethal, genetic, multisystem disorder characterized by the presence of occipital encephalocele, cystic kidneys, and polydactyly. It is an autosomal recessive disorder, meaning that both parents must carry and pass on the defective gene for a child to be affected. The syndrome is named after Johann Friedrich Meckel and Georg Bartsch Gruber, who first described the condition in the 19th century. == Clinical Fe..."
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