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Wiedemann-Rautenstrauch syndrome
rareWiedemann-Rautenstrauch syndrome is a very rare disorder with features of premature aging recognizable at birth, decreased subcutaneous fat, hypotrichosis, relative macrocephaly and dysmorphism.
- Identifiers
- MONDO:0009910 OMIM:264090Orphanet:3455
- Part of
- POLR3A-related disorderDevelopmental anomaly of metabolic originHereditary lipodystrophyMultiple congenital anomalies/dysmorphic syndrome-intellectual disabilityOsteogenesis imperfecta and a reduction of bone mineral density.Progeroid syndromeSyndromic disease
- Also known as
- neonatal progeroid syndrome · progeroid syndrome neonatal · Wiedemann Rautenstrauch Syndrome
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