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Wiedemann-Rautenstrauch syndrome | RareConnect | RareConnect.io

/syndromic disease

/multiple congenital anomalies/dysmorphic syndrome-intellectual disability

/developmental anomaly of metabolic origin

/Wiedemann-Rautenstrauch syndrome

Wiedemann-Rautenstrauch syndrome

Rare Disease

MONDO:0009910

Also Known As

Wiedemann Rautenstrauch SyndromeWiedemann-Rautenstrauch syndromeneonatal progeroid syndromeWiedemann Rautenstrauch syndromeprogeroid syndrome neonatalprogeroid syndrome, neonatal

Definition

Wiedemann-Rautenstrauch syndrome is a very rare disorder with features of premature aging recognizable at birth, decreased subcutaneous fat, hypotrichosis, relative macrocephaly and dysmorphism.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:264090 ↗

Orphanet

Orphanet:3455 ↗

GARD

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