Wiedemann-Rautenstrauch syndrome: report of a variant case.

doi:10.1002/ajmg.a.35336

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Article

Wiedemann-Rautenstrauch syndrome: report of a variant case.

American journal of medical genetics. Part A - 1 Jun 2012

Kiraz Aslihan, Ozen Samim, Tubas Filiz, Usta Yusuf, Aldemir Ozgur, Alanay Yasemin

Abstract excerpt

Wiedemann-Rautenstrauch syndrome (WRS) is a rare autosomal recessive disorder that includes premature aging phenotype at birth. The condition is also known as a neonatal progeroid syndrome. Up to now only a few published case reports have been documented. The syndrome is characterized by progeroid appearance, decreased subcutaneous fat, hypotrichosis, macrocephaly, and in some natal teeth. We describe a new...

Topics

Child, Preschool
Facies
Female
Fetal Growth Retardation
Humans
Phenotype
Progeria

Source

Open in PubMed

Identifiers

PMID: 22585414
DOI: 10.1002/ajmg.a.35336

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

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