Meckel syndrome is a disorder with severe signs and symptoms that affect many parts of the body. The most common features are enlarged kidneys with ...
Meckel syndrome (also known as Meckel–Gruber Syndrome, Gruber Syndrome, Dysencephalia Splanchnocystica) is a rare, lethal, ciliopathic, genetic disorder ...
The first reports of Meckel-Gruber syndrome (MKS) were published in 1822 by Johann Friedrich Meckel. G.
Important It is possible that the main title of the report Meckel Syndrome is not the name you expected. Please check the synonyms listing to find the ...
Meckel-Gruber syndrome is an inherited genetic disorder. Both parents must carry copies of the defective gene for their child to develop the syndrome.
Meckel-Gruber syndrome (MKS) is an autosomal recessive disorder, characterized by a combination of renal cysts and variably associated with features including ...
Meckel-Gruber syndrome (MGS) is classically characterised by the triad of: renal cystic dysplasia (multiple renal cysts) (present most cases) occipital encephalocoele ...
1. Ahdab-Barmada, M., Claassen, D. A distinctive triad of malformations of the central nervous system in the Meckel-Gruber syndrome. J. Neuropath.
A rare, lethal, autosomal recessive inherited syndrome characterized by pulmonary hypoplasia, central nervous system malformations, and hepatic malformations.
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