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Hypospadias - intellectual disability, Goldblatt type

ORPHA2261
Synonym(s) Goldblatt-Wallis syndrome
Prevalence -
Inheritance -
Age of onset -
ICD-10
  • Q87.8
OMIM
UMLS -
MeSH -
MedDRA -

Summary

Hypospasdias – intellectual deficit, Goldblatt type is a very rare multiple congenital anomalies syndrome described in three brothers of one South-African family, and characterized by hypospadias and intellectual deficit, in association with mirocephaly, craniofacial dysmorphism, joint laxity and beaked nails.


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