Autosomal recessive disorder characterized by HYALINE deposition in the skin, bone, gastrointestinal tract, muscles and glands; multiple subcutaneous skin nodules; GINGIVAL HYPERTROPHY; and joint CONTRACTURES. Mutations in the capillary morphogenesis protein-2 are associated with the disorder.
Also Known As:
Fibromatosis Hyalinica Multiplex Juvenilis; Fibromatosis Juvenile Hyaline; Fibromatosis, Juvenile Hyaline; Hyaline Fibromatosis Juvenile; Hyalinosis, Systemic Juvenile; Infantile Systemic Hyalinosis; Juvenile Hyaline Fibromatosis; Juvenile Hyalinosis; Murray Syndrome; Puretic Syndrome; Systemic Hyalinosis; Fibromatosis Syndrome, Hyaline; Fibromatosis Syndromes, Hyaline; Hyaline Fibromatosis Syndromes; Hyaline Fibromatosis, Juvenile; Hyalinoses, Infantile Systemic; Hyalinoses, Juvenile; Hyalinoses, Systemic; Hyalinoses, Systemic Juvenile; Hyalinosis, Infantile Systemic; Hyalinosis, Juvenile; Infantile Systemic Hyalinoses; Juvenile Hyaline Fibromatoses; Juvenile Hyalinoses; Juvenile Hyalinoses, Systemic; Juvenile Hyalinosis, Systemic; Puretic Syndromes; Syndrome, Hyaline Fibromatosis; Syndrome, Murray; Syndrome, Puretic; Syndromes, Hyaline Fibromatosis; Syndromes, Puretic; Systemic Hyalinoses; Systemic Hyalinoses, Infantile; Systemic Hyalinosis, Infantile; Systemic Juvenile Hyalinoses; Systemic Juvenile Hyalinosis; Hyalinosis, Systemic