Wiedemann-Steiner syndrome

Disease Export to PDF
Name:
Wiedemann-Steiner syndrome
Description:
A rare, genetic multiple congenital anomalies/dysmorphic syndrome characterized by short stature, hypertrichosis (most commonly of the back or elbow regions), facial dysmorphism, behavioral problems, developmental delay and, most commonly, mild to moderate intellectual disability.
ORPHAcode:
319182
Synonyms:
Hypertrichosis-short stature-facial dysmorphism-developmental delay syndrome
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14