44 top medical experts on Type IIA Autosomal Recessive Cutis Laxa across 8 countries, including 1 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Type IIA Autosomal Recessive Cutis Laxa: A rare, genetic, dermis elastic tissue disease characterized by redundant, overfolded skin of variable severity, ranging from wrinkly skin to cutis laxa associated with pre- and post-natal growth retardation, hypotonia, mild to moderate developmental delay, late closure of anterior fontanelle, and craniofacial dysmorphism (including microcephaly, hypertelorism, downslanting palpebral fissures, large, prominent nasal root with funnel nose, small, low-set ears, long philtrum, drooping facial skin). Additional manifestations may include seizures, intellectual disability, congenital hip dislocation, inguinal hernia, and cortical and cerebellar malformations. Pretibial pseudo-ecchymotic skin lesions have occasionally been associated.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Synonyms: ARCL2A,  Cutis Laxa With Bone Dystrophy,  Cutis Laxa With Growth And Developmental Delay,  Cutis Laxa With Joint Laxity And Retarded Development,  Cutis Laxa With Or Without Congenital Disorder Of Glycosylation,  Debre Type Cutis Laxa


  

        

                    


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