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Cutis laxa (CL) is a rare connective tissue disorder which may be inherited or acquired. It is characterized by a loose skin. Inherited forms are autosomal dominant, autosomal recessive and X-linked recessive. Congenital cutis laxa may present with variable systemic involvement e.g (gastrointestinal, CNS and cardiopulmonary) determining a worst prognosis. Acquired forms of this disease have been associated with a past inflammatory skin disorder. We report a 4 year old boy with a congenital cutis laxa. He was admitted for vomiting and constipation. Diagnosis of cutis laxa is typically made by physical examination and associated extra cutaneous finding. Cutis laxa is a rare disorder, diagnosed clinically although there is wide clinical and genetic heterogeneity.

MADIHA NAZ, BUSHRA IQBAL, NUSRAT HUSSAIN BUZDAR, Shahzad Malana, Fauzia Zafar, Faiza Anam. (2021) Cutis Laxa in Pediatrics with Hiatal Hernia: A Rare Presentation, Pakistan Pediatric Journal, Volume 45, Issue 2.
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