Calciphylaxis is a serious condition characterized by the blockage of blood vessels due to calcium buildup in their walls, leading to ischemia and tis...

Calciphylaxis cutis is a serious condition characterized by painful skin ulcerations due to the calcification of small and medium-sized cutaneous arte...

calloso-genital dysplasia is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Calvarial doughnut lesions-bone fragility syndrome is characterized by multiple doughnut-shaped hyperostotic or osteosclerotic lesions of the calvaria...

Calvarial doughnut lesions with bone fragility and spondylometaphyseal dysplasia is an extremely rare condition. Because few cases have been documente...

CAMOS syndrome is a rare condition that has been reported in a large Lebanese family. It is characterized by a non-progressive congenital ataxia, seve...

Campomelia, Cumming type is an extremely rare condition characterized by limb defects and various multivisceral anomalies. It is inherited in an autos...

Campomelic dysplasia is a very rare skeletal dysplasia that affects the development of bones, airway structures, and several internal organs. Most cas...

Camptobrachydactyly is an extremely rare brachydactyly syndrome characterized by short, broad hands and feet, alongside congenital flexion contracture...

Camptodactyly-arthropathy-coxa vara-pericarditis syndrome (also known as CACP syndrome) is a rare genetic rheumatologic condition that primarily affec...

camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye is an extremely rare condition. Because few cases have been documented, detaile...

Camptodactyly of fingers is a rare, genetic condition characterized by a painless, permanent flexion contracture at the proximal interphalangeal joint...

Camptodactyly syndrome, Guadalajara type 1 is an extremely rare condition. Because few cases have been documented, detailed clinical information is li...

Camptodactyly syndrome, Guadalajara type 2 is an extremely rare condition. Because few cases have been documented, detailed clinical information is li...

Camptodactyly syndrome, Guadalajara type 3 is a rare genetic bone development disorder characterized by hand camptodactyly and associated facial dysmo...

Camptodactyly-tall stature-scoliosis-hearing loss syndrome (CATSHL) is a very rare hereditary condition that primarily affects the skeleton, joints, s...

Camptodactyly-taurinuria syndrome is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia is an extremely rare condition. Because few cases have been documented, detailed...

Camptomelic syndrome, long-limb type is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Camurati-Engelmann disease (CED) is an inherited bone dysplasia in which the shafts of the long bones, skull, spine, and pelvis become abnormally thic...