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149 Possible Causes for Ehlers Danlos Syndrome, Livedo Reticularis, Marfanoid Habitus

  • Homocystinuria

    ( E34.5- ) congenital adrenal hyperplasia ( E25.0 ) Ehlers-Danlos syndrome ( Q79.6 ) hemolytic anemias attributable to enzyme disorders ( D55.- ) Marfan's syndrome ( Q87.4[] habitus, osteoporosis, attention deficit and hyperactivity disorder.[] reticularis Atrophic scars on arms and hands Telangiectasia What causes homocystinuria?[]

  • Ehlers Danlos Syndrome

    […] type, 2 Ehlers-Danlos syndrome, type 2 atypical Ehlers-Danlos syndrome, type 3 Ehlers-Danlos syndrome, type 4 Ehlers-Danlos syndrome, type 4 variant Ehlers-Danlos syndrome[] habitus.[] […] irritable bowel syndrome) Gastroparesis Nerve compression disorders (carpal tunnel syndrome, acroparesthesia, neuropathy) Vascular skin conditions: Raynaud's phenomenon, Livedo[]

  • Hypermobility Syndrome

    INTRODUCTION: An increased risk of preterm birth in women with joint hypermobility syndrome or Ehlers-Danlos syndrome is suspected.[] Initially it included things like mild variants of the skin changes described above, and the often-found body shape called the marfanoid habitus (see below).[] Characteristics of FTAA are: thoracic aortic aneurysms, patent ductis arteriosus, non-thoracic aneurysms, livedo reticularis, and iris flocculi.[]

  • Ehlers-Danlos Syndrome due to Tenascin-X Deficiency

    Prognosis - Ehlers-Danlos syndrome caused by tenascin-X deficiency Not supplied. Treatment - Ehlers-Danlos syndrome caused by tenascin-X deficiency Not supplied.[] Marfanoid habitus is absent.[] Reticularis; Poor Connective Tissue integrity (dislocations, bruising, bleeding, petechaie, calcific aortic valves, Mitral Valve Prolapse); Dry eyes; Tinnitis; Subcutaneous[]

  • Ehlers-Danlos Syndrome, Type 3

    What are the types of Ehlers-Danlos syndromes?[] Marfan patients generally have a body type called a Marfanoid body habitus.[] […] irritable bowel syndrome) Gastroparesis Nerve compression disorders (carpal tunnel syndrome, acroparesthesia, neuropathy) Vascular skin conditions: Raynaud's phenomenon, Livedo[]

  • Ehlers-Danlos Syndrome, Type 6

    Causes - Ehlers-Danlos syndrome - type VIa - kyphoscoliosis Prevention - Ehlers-Danlos syndrome - type VIa - kyphoscoliosis Diagnosis - Ehlers-Danlos syndrome - type VIa -[] Other findings may include: marfanoid habitus; microcornea; and radiologically considerable osteopenia.[] reticularis .[]

  • Aortic Dissection

    The Ehlers-Danlos syndromes, rare types.[] ACTA2 mutations have been identified in 14% of TAA/D and have been associated with livedo reticularis, patent ductus arteriosus, and bicuspid aortic valve. 3 If a specific[] […] and Ehlers-Danlos syndrome) and rare genetic disorders Heart surgery or procedures Pregnancy Swelling of the blood vessels due to conditions such as arteritis and syphilis[]

  • Ehlers-Danlos Syndrome with Periventricular Heterotopia

    TY - JOUR T1 - Ehlers-Danlos syndrome with subependymal periventricular heterotopias.[] Osteopenia/osteoporosis, blue sclerae, hernia, pectus deformity, marfanoid habitus, clubfoot, and refractive errors are also frequently observed and form the minor criteria[] Macrocephaly Cutis marmorata telangiectatica congenita. Report of five cases and review of the literature. Clinical Dysmorphology, 9 (1), 1-9. Robertson, S.[]

  • Cutis Laxa-Marfanoid Syndrome

    HONselect - Ehlers-Danlos Syndrome Disease, EhlersDanlos - Ehlers Danlos Disease - Ehlers Danlos Syndrome - Syndrome, Ehlers-Danlos.[] Part A 127a(3): 310-312, 2004 X linked mental retardation and marfanoid habitus . Journal de Genetique Humaine 36(1-2): 123-128, 1988[] reticularis Congenital melanosis Congenital oculocutaneous hypopigmentation Congenital oculocutaneous hypopigmentation Congenital palmoplantar and perioral keratoderma of[]

  • Melhem-Fahl Syndrome

    Ehlers-Danlos syndrome, classic type Retrieved: 27-07-2015 Ehlers-Danlos syndrome, classic type (cEDS) is a form of Ehlers-Danlos syndrome (EDS; see this term) that affects[] habitus Microcephaly hiatus hernia nephrotic syndrome Microcephaly hypergonadotropic hypogonadism short stature Microcephaly immunodeficiency lymphoreticuloma Microcephaly[] marmorata juvenile form Spastic Paraplegia Hereditary telangiectatica congenita PUJO 11p deletion syndrome Niemann-Pick disease chronic Megalocephaly cutis marmorata neuronopathic[]

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