synovial chondromatosis

A rare hereditary disorder marked by various combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and sometimes learning disability or mental retardation.

A paediatric medical disorder characterised by gastrointestinal symptoms and associated neurological features.

A form of palmoplantar keratoderma of the palms and soles, with flexion deformity of the digits, that begins in infancy.

A form of palmoplantar keratoderma with scleroatrophy.

A form of palmoplantar keratoderma characterized by a honeycomb pattern, sometimes associated with hearing loss.

A rare disease characterised by chronic hives and periodic fever, bone and joint pain (sometimes with joint inflammation), weight loss, malaise, fatigue, swollen lymph glands and enlarged spleen and liver.

Bazex-Dupré-Christol syndrome / acrokeratosis paraneoplastica of Bazex

A form of striate palmoplantar keratoderma with woolly hair and cardiomyopathy.

A rare form of palmoplantar keratoderma.