A congenital neurodegenerative syndrome with various physical anomalies, including severe midface retraction, and retarded growth and mental development.

A loss of sensation and motor function caused by the lateral hemisection of the spinal cord.

congenital self-healing reticulohistiocytosis: a self-limited form of Langerhans cell histiocytosis

A rare disease characterized by difficulty in swallowing, iron-deficiency anemia, and esophageal webs.

An X-linked recessive connective tissue disorder caused by a deficiency in the transport of copper, and leading to the formation of projections on the back of the skull.

Freeman-Sheldon syndrome

A rare severe form of distal arthrogryposis.

acrodermatitis enteropathica

eosinophilic granulomatosis with polyangiitis

plural of toxic shock syndrome