Number of the records: 1
dysplázia kampomelická
Record number d055036 Date 06.06.2025 Type M Topical term dysplázia kampomelická See also (Later heading) Pierre Robinov syndróm
(Skutočné meno) Pierre Robinov syndróm
UDC C05.660.142C16.131.621.142 Note A congenital disorder of CHONDROGENESIS and OSTEOGENESIS characterized by hypoplasia of endochondral bones. In most cases there is a curvature of the long bones especially the TIBIA with dimpling of the skin over the bowed areas, malformation of the pelvis and spine, 11 pairs of ribs, hypoplastic scapulae, club feet, micrognathia, CLEFT PALATE, tracheobronchomalacia, and in some patients male-to-female sex reversal (SEX REVERSAL, GONADAL). Most patients die in the neonatal period of respiratory distress. Campomelic dysplasia is associated with haploinsufficiency of the SOX9 TRANSCRIPTION FACTOR gene. 
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Number of the records: 1