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Results 1 - 4 of 4 for Arthrogryposis multiplex congenita
  1. X-linked infantile spinal muscular atrophy 
    ... pass X-linked traits to their sons. AMCX1 Arthrogryposis multiplex congenita, distal, X-linked Arthrogryposis, X-lined, type I ... muscular atrophy, X-linked lethal infantile X-linked arthrogryposis multiplex congenita X-linked arthrogryposis type I X-linked lethal ...
    https://medlineplus.gov/...-linked-infantile-spinal-muscular-atrophy - Genetics
  2. Multiple pterygium syndrome 
    Multiple pterygium syndrome is a condition that is evident before birth with webbing of the skin (pterygium) at the joints and a lack of muscle movement (akinesia) ...
    https://medlineplus.gov/.../condition/multiple-pterygium-syndrome - Genetics
  3. Arthrogryposis (Nemours Foundation)  
    arthrogryposis, AMC, arthrogryposis multiplex congenita, joints, stiff joints, contractures, clubfoot, splints, splinting, braces, bracing, occupational therapy, physical therapy, and orthopedic surgery, loss of ...
    https://kidshealth.org/en/parents/arthrogryposis.html - External Health Links
  4. Sheldon-Hall syndrome 
    ... no history of the disorder in their family. Arthrogryposis multiplex congenita, distal, type 2B DA2B Distal arthrogryposis type 2B SHS National Organization for Rare Disorders ( ...
    https://medlineplus.gov/genetics/condition/sheldon-hall-syndrome - Genetics