Wiedemann-Rautenstrauch syndrome
Name: |
Wiedemann-Rautenstrauch syndrome
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Description: |
A rare multiple congenital anomalies/dysmorphic syndrome characterized by marked prenatal and postnatal growth retardation, decreased subcutaneous fat, hypotrichosis, relative macrocephaly and an unusual face. Mild to moderate intellectual disability is common.
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ORPHAcode: |
3455
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Synonyms: |
Neonatal progeroid syndrome
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XREF(s): | |
Analyte(s): | |
Created: |
13 May 2019 - 01:02
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Changed: |
22 Jun 2023 - 16:14
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