Congenital Limb Malformations (Subscribe)

Web site of a support group for this joint condition Patient Provider

Cleft lip and palate, hypoplasia and/or syndactyly. Mental retardation. Orocraniodigital syndrome is an extremely rare inherited disorder characterized by multiple malformations of the head and face (craniofacial area) and the fingers and toes (digits). Major characteristics may include a vertical groove in the upper lip (cleft lip) and/or the inside,...

Mental and growth retardation, polysyndactyly. Nord Database

distinctive malformations of the head and facial (craniofacial) region and defects of the hands and feet. In some instances, mental retardation. unusually broad thumbs and great toes, short fingers, and/or partial to complete fusion (syndactyly) of certain fingers and toes (digits). Most commonly, there is complete fusion of bones within...

Also known as Acrocephalopolysyndactyly Type II. Craniosynostosis and polysyndactyly. NORD Database

PROXIMAL FEMORAL FOCAL DIFICIENCY

Blount's Disease, The Alfred I. duPont Institute.

malformations of the fingers and toes, and/or underdevelopment of portions of the face (midface hypoplasia); ocular hypertelorism

Dwarfism, Madelung Deformity. NORD Database

short limb dwarfism, additional fingers and/or toes (polydactyly), abnormal development of fingernails and, in over half of the cases, congenital heart defects. NORD Database

Vertebral and Craniofacial abnormalities. NORD Database

malformations of the head and face, abnormalities of the hands and feet, and congenital heart disease. ACPS type IV. Nord Database

Craniofacial malformations, polysyndactyly. NORD Database

Craniofacial abnormalities. Broad great toes

Polydactyly, encephalocoele and polcystic kidneys. NORD database