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伴有血小板增多症和先天性髋关节脱位的CHILD综合征:来自印度的一例病例报告。

CHILD syndrome with thrombocytosis and congenital dislocation of hip: A case report from India.

作者信息

Chander Ram, Varghese Bincy, Jabeen Masarat, Garg Taru, Jain Manjula

机构信息

Department of Dermatology, Venereology and Leprosy, Lady Hardinge Medical College, New Delhi, India.

出版信息

Dermatol Online J. 2010 Aug 15;16(8):6.

Abstract

Congenital Hemidysplasia with Ichthyosiform Nevus and Limb Defects (CHILD) is a very rare entity inherited as an X-linked trait. The cutaneous lesions are characteristic and usually involve the right side of the body. We report a case of CHILD syndrome in an Indian child affecting the left side with various other associations not yet described in the literature, such as thrombocytosis and congenital dislocation of the hip. The rarity of the syndrome prompted us to report this case.

摘要

先天性半侧发育不良伴鱼鳞病样痣和肢体缺损(CHILD)综合征是一种非常罕见的以X连锁方式遗传的疾病。其皮肤损害具有特征性,通常累及身体右侧。我们报告一例印度儿童的CHILD综合征,该患儿病变累及左侧身体,还伴有血小板增多症和先天性髋关节脱位等多种尚未见文献报道的其他关联表现。该综合征的罕见性促使我们报告此病例。

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