NPHP3-related Meckel-like syndrome

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Name:
NPHP3-related Meckel-like syndrome
Description:
NPHP3-related Meckel-like syndrome is a rare, genetic, syndromic renal malformation characterized by cystic renal dysplasia with or without prenatal oligohydramnios, central nervous system abnormalities (commonly Dandy-Walker malformation), congenital hepatic fibrosis, and absence of polydactyly.
ORPHAcode:
3032
Synonyms:
Goldston syndrome
Meckel syndrome type 7
Meckel-like syndrome type 1
Renal-hepatic-pancreatic dysplasia-Dandy-Walker cysts syndrome
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Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14