Keppen–Lubinsky syndrome

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Keppen–Lubinsky syndrome
Synonyms Generalized lipodystrophy-progeroid features-severe intellectual disability syndrome
Autosomal dominant - en.svg
This condition is inherited in an autosomal dominant manner
Classification and external resources
ICD-10 E88.1
OMIM 614098
Orphanet 435628

Keppen–Lubinsky syndrome is an extremely rare congenital disorder.The minimal clinical criteria for the Keppen–Lubinsky syndrome are as follows: normal growth parameters at birth, postnatal growth failure, peculiar facial appearance with skin tightly adherent to facial bones, generalized lipodystrophy and development delay.

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