Arcl2 progeroid type

A rare autosomal recessive disorder associated with abnormalities in bone maturation, and lipids and hormone metabolism and characterized by intrauterine growth retardation, failure to thrive, short stature, a progeroid appearance, hypotonia, variable mental impairment, and death in childhood. Its cause is unknown.

Disease Alternative Name

wiedemann-rautenstrauch syndrome
neonatal progeroid syndrome

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