Abstract
Wiedemann Rautenstauch (WR) syndrome is a rare autosomal recessive neonatal progeroid syndrome with only few published case reports. We describe a neonate showing clinical features of WR syndrome with peeling of skin, and presented with weak cry and breathing difficulty since birth.
MeSH terms
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Fatal Outcome
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Female
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Fetal Growth Retardation / diagnosis*
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Fetal Growth Retardation / pathology
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Fetal Growth Retardation / physiopathology
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Humans
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Infant, Newborn
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Progeria / diagnosis*
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Progeria / pathology
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Progeria / physiopathology
Supplementary concepts
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Progeroid syndrome, neonatal