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Familial Peeling Skin Syndrome

Authors

  • SADAF FASIH ZUHA NAEEM TARIQ RASHID

Keywords:

Deciduous skin, keratolysis exfoliativa congenita, familial peeling skin syndrome

Abstract

Peeling skin syndrome (PSS) is a rare form of icthyosis with an autosomal recessive inheritance that exhibits superficial painless, continual, or seasonal exfoliation. The syndrome generally appears at birth or in infancy. A 12 year old female child born of consanguineous marriage presented with generalized periodic peeling of skin since 2 years of age. It was associated with itching, seasonal variations and erythema. The child also had mental retardation, attention deficit hyperactivity syndrome and ocular albinism. Her younger brother was also affected from the similar disease.

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Published

2018-07-15

How to Cite

1.
ZUHA NAEEM TARIQ RASHID SF. Familial Peeling Skin Syndrome. J Fatima Jinnah Med Univ [Internet]. 2018 Jul. 15 [cited 2024 May 18];5(1). Available from: https://www.jfjmu.com/index.php/ojs/article/view/548