669 Possible Causes for Laurence Moon Syndrome

  • Polydactyly

    It was later erroneously coupled with another disorder described by Laurence and Moon, and was consequently referred to as LaurenceMoon–Biedl syndrome.[academic.oup.com] Causes Causes may include: Asphyxiating thoracic dystrophy Carpenter syndrome Ellis-van Creveld syndrome (chondroectodermal dysplasia) Familial polydactyly Laurence-Moon-Biedl[mountsinai.org] The cardinal manifestations of Bardet–Biedl syndrome, a form of Laurence– Moon–Biedl syndrome.[academic.oup.com]

  • Paraplegia

    MAG * SPG75 NIPA1 SPG6 NT5C2 SPG45 PGAP1 * intellectual disability PLP1 SPG2 Pelizaeus-Merzbacher disease PNPLA6 SPG39 Boucher-Neuhäuser syndrome, Oliver-McFarlane/Laurence-Moon[invitae.com] ., syndromic) and uncomplicated forms.[invitae.com] syndrome RAB3GAP2 * Warburg Micro syndrome-2, Martsolf syndrome REEP1 SPG31 distal hereditary motor neuropathy REEP2 * SPG72 RTN2 SPG12 SACS ARSACS autosomal recessive spastic[invitae.com]

  • Hypogonadism

    CHH is also a feature of several syndromes including the Prader-Willi, Bardet-Biedl, Laurence-Moon and CHARGE syndromes (see these terms).[orpha.net] […] disease, Laurence-Moon-Biedl disease, Lowe syndrome, Prader-Willi syndrome . hy·po·go·nad·ism ( hī'pō-gō'nad-izm ) Inadequate gonadal function, as manifested by deficiencies[medical-dictionary.thefreedictionary.com] Some specific conditions associated with diabetes mellitus, such as hemachromatosis, and the Laurence-Moon Biedl, Alstrom, and Cushing syndromes, also typically produce hypogonadism[encyclopedia.com]

  • Retinitis Pigmentosa

    Short stature, renal dysfunction, and polydactyly are some signs of Bardet-Biedl syndrome or Laurence-Moon syndrome when associated with pigmentary retinopathy.[patient.info] Associated systemic syndromes include Bassen-Kornzweig, Kearns-Sayre, Laurence-Moon-Bardet-Biedl, Refsum's and Usher's.[medical-dictionary.thefreedictionary.com] RP and hearing loss also are associated with Waardenburg's syndrome, Alström's syndrome , Alport's syndrome , Refsum's syndrome , and other systemic conditions, all of which[patient.info]

  • Mental Retardation
  • Hypodontia
  • Syndactyly
  • Diabetes Insipidus
  • Laurence Moon Syndrome

    Laurence-Moon syndrome [lô′rəns mo̅o̅n] Etymology: John Zachariah Laurence, British ophthalmologist, 1830-1874; Robert C.[medical-dictionary.thefreedictionary.com] LaurenceMoon syndrome ( LMS ) is a rare autosomal recessive LaurenceMoon–Bardet–Biedl Syndrome Medical notes and references[en.wikipedia.org] Homepage Rare diseases Search Search for a rare disease Laurence-Moon syndrome Disease definition Laurence-Moon syndrome (LMS) is a very rare genetic multisystemic disorder[orpha.net]

  • Donohue Syndrome

    ICD 10 Q … Wikipedia Bardet–Biedl syndromeLaurence Moon Biedl syndrome and Laurence Moon Biedl Bardet redirect here.[dic.academic.ru] Donohue syndrome Donohue syndrome .[dic.academic.ru] Смотреть что такое "Donohue syndrome" в других словарях: Donohue syndrome — Classification and external resources insulin receptor OMIM 246200 … Wikipedia Donohue syndrome[dic.academic.ru]

Further symptoms