Conradi-Hünermann disease

chon·dro·dys·pla·si·a cal·ci·f'i·cans con·gen·'i·ta

[MIM*118650] autosomal dominant inheritance characterized by asymmetric calcifications and dysplastic skeletal changes, less frequent occurrence of congenital cataracts and ichthyosis compared with other forms, and relatively good prognosis. Synonym(s): Conradi disease, Conradi-Hünermann disease

Conradi-Hünermann disease

(1) Chondrodysplasia punctata (type I), OMIM:118650. 
(2) X-linked dominant chondrodysplasia punctata (type II), OMIM:302960.

Conradi,

Erich, German physician, 1882–. Conradi disease - congenital shortening of the humerus and femur, with stippled epiphyses, high-arched palate, cataracts, erythroderma in the newborn, and scaling followed by follicular atrophoderma. Synonym(s): chondrodystrophia congenita punctata; Conradi-Hunermann disease; Conradi syndromeConradi syndrome - Synonym(s): Conradi diseaseConradi-Hunermann disease - Synonym(s): Conradi disease

Hunermann,

Carl, German pediatrician, 1900-1943. Conradi-Hunermann disease - Synonym(s): Conradi disease