Upington disease, also called Perthes-like hip disease, enchondromata, ecchondromata, and familial dyschondroplasia is an extremely rare autosomal dominant malformation disorder having only one published source claiming its existence on one family in three generations from South Africa.
It has only one published source claiming its existence in three generations of one family from South Africa. Upington disease, also called Perthes-like hip disease, enchondromata, ecchondromata, and familial dyschondroplasia, is an extremely rare autosomal dominant malformation disorder.
Upington disease, also called Perthes-like hip disease, enchondromata, ecchondromata, and familial dyschondroplasia, is an extremely rare autosomal dominant malformation disorder. It has only one published source claiming its existence in three generations of one family from South Africa.
Upington disease, also called Perthes-like hip disease, enchondromata, ecchondromata, and familial dyschondroplasia, is an extremely rare autosomal dominant malformation disorder. It has only one published source claiming its existence in three generations of one family from South Africa.