Holoprosencephaly-radial heart renal anomalies syndrome

Orpha code: 3186OMIM code: 184705

Definition

A rare multiple congenital anomalies syndrome characterised by holoprosencephaly, predominantly radial limb deficiency (absent thumbs, phocomelia), heart defects, kidney malformations and absence of gallbladder. Variable manifestations include vertebral anomalies, cleft lip/palate, microphthalmia, absent nose, dysplastic ears, hearing loss, colobomas of the iris and retina and/or bifid uvula.

Disease data
Classification

Malformation syndrome

Synonyms
Steinfeld syndrome
Zespół Steinfelda
ORPHA code
3186
OMIM code
184705
ICD10 code
Q87.8
ICD11 code
-

No additional description.

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