20 top medical experts on X-linked distal Arthrogryposis multiplex congenita across 4 countries, including 3 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. X-linked distal Arthrogryposis multiplex congenita: A rare form of spinal muscular atrophy characterized by the neonatal onset of severe hypotonia, areflexia, profound weakness, multiple congenital contractures, facial dysmorphic features (myopathic face with open, tent-shaped mouth), cryptorchidism, and mild skeletal abnormalities (i.e. kyphosis, scoliosis), that is often preceded by polyhydramnios and reduced fetal movements in utero and followed by bone fractures shortly after birth. Muscle weakness is progressive and chest muscle involvement eventually leads to ventilatory insufficiency and respiratory failure.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: X-linked distal AMC,  Amcx1,  Type I X-Linked Arthrogryposis,  Smax2,  Infantile X-Linked Spinal Muscular Atrophy,  X-Linked 2 Spinal Muscular Atrophy,  X-Linked Lethal Infantile Spinal Muscular Atrophy,  Xlsma


  

        

                    


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