Abstract:This case report describes the rare variant of autosomal recessive cutis laxa with bone dystrophy in a Sudanese child. The clinical features include cutis laxa, growth and development retardation, facial dysmorphism, hyperextensible joints, dislocation of the hips and a large umbilical hernia.
“…In literature, it's reported that three intermarriage family with CLS had 5 hip dislocations . [23] In the contrast of previously mentioned findings of the etiopathogenesis, we believe hip dysplasia of our patient may be incidental.…”
Congenital CLS is a genetical syndrome which is inherited as autosomal dominant and recessive form. [7] Autosomal dominant form is more benign. Parents of the patient with
“…In literature, it's reported that three intermarriage family with CLS had 5 hip dislocations . [23] In the contrast of previously mentioned findings of the etiopathogenesis, we believe hip dysplasia of our patient may be incidental.…”
Congenital CLS is a genetical syndrome which is inherited as autosomal dominant and recessive form. [7] Autosomal dominant form is more benign. Parents of the patient with
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