Çocuk Sağlığı ve Hastalıkları Dergisi 2004 , Vol 47 , Num 4
A case report of rhizomelic chondrodysplasia punctata with hypospadias.
Semra Çetinkaya1, Fikriye Sarıkayalar2, Zeynep Alev Özön3, Sevim Balcı4
Hacettepe Üniversitesi Tıp Fakültesi 1Pediatri Uzmanı, 2Pediatri Profesörü, 3Pediatri Yardımcı Doçenti, 4Pediatri Profesörü Çetinkaya S, Sarıkayalar F, Özön ZA, Balcı S.(Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey). A case report of rhizomelic chondrodysplasia punctata with hypospadias. Çocuk Sağlığı ve Hastalıkları Dergisi 2004; 47: 273-276.

Rhizomelic chondrodysplasia punctata is characterized by chondrodysplasia punctata (CDP), ichthyosis, cataracts, and rhizomelic or rhizomesomelic short stature. CDP is the hallmark of the disease, characterized by abnormal punctate calcifications in the dystrophic epiphyseal cartilages, as well as other cartilagenous structures. The disorder belongs to a rare group of skeletal dysplasias, and the incidence is reported to be 1 per 100,000 live births. Two other patients have been reported from Turkey before. Our patient is the first report of a case with chondrodysplasia punctata with hypospadias. Anahtar Kelimeler : kondrodisplazia punktata, hipospadias, katarakt, lateral ventrikül dilatasyonu,chondrodysplasia punctata, hypospadias, cataracts, dilatation of lateral ventriculus.

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