680 Possible Causes for Laurence Moon Syndrome

  • Anterior Pituitary Disease

    […] other than HGH Isolated follitropin deficiency Isolated gonadotropin deficiency Isolated lutropin deficiency Isolated prolactin deficiency Isolated thyroliberin deficiency Laurence-Moon[icd9data.com] . · Kallmann syndrome (isolated hypogonadotropic hypogonadism, associated with defects of smell, X-linked). · Laurence-Moon-Bardet-Bidel Syndrome (autoso­mal recessive, mental[medicscientist.com] syndrome LH - luteinizing hormone deficiency Luteinizing hormone deficiency Pituitary disorder, anterior Primary hypogonadism Progressive cerebellar ataxia with hypogonadism[icd9data.com]

  • Nephronophthisis

    Associated Diseases: Retinitis pigmentosa (Senior-Løken syndrome) Laurence-Moon-Bardet-Biedl syndrome (obesity, debility, polydactyly, retinitis pigmentosa and hypogenitalism[urology-textbook.com]

  • Retinitis Pigmentosa 26

    Short stature, renal dysfunction, and polydactyly are some signs of Bardet-Biedl syndrome or Laurence-Moon syndrome when associated with pigmentary retinopathy.[patient.info] 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]

  • Retinitis Pigmentosa 7

    Short stature, renal dysfunction, and polydactyly are some signs of Bardet-Biedl syndrome or Laurence-Moon syndrome when associated with pigmentary retinopathy.[patient.info] 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]

  • 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] For example, polydactyly is a characteristic of Meckel syndrome and Laurence-Moon-Biedl syndrome.[medical-dictionary.thefreedictionary.com]

  • Retinitis Pigmentosa 41

    Short stature, renal dysfunction, and polydactyly are some signs of Bardet-Biedl syndrome or Laurence-Moon syndrome when associated with pigmentary retinopathy.[patient.info] RP patients affected with Laurence-Moon-Biedl-Syndrome (LMB) constituted about 3.3 % of the sample.[ijo.in] 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]

  • Hyperphosphatasia-Intellectual Disability Syndrome 1

    This syndrome has been distinguished as a separate entity from LAURENCE-MOON SYNDROME.[bioportfolio.com] This syndrome was previously referred to as Laurence-Moon-Biedl syndrome until BARDET-BIEDL SYNDROME was identified as a distinct entity.[bioportfolio.com] Laurence-moon Syndrome An autosomal recessive condition characterized by hypogonadism; spinocerebellar degeneration; MENTAL RETARDATION; RETINITIS PIGMENTOSA; and OBESITY.[bioportfolio.com]

  • Hyperphosphatasia - Intellectual Disability Syndrome

    This syndrome has been distinguished as a separate entity from LAURENCE-MOON SYNDROME.[bioportfolio.com] This syndrome was previously referred to as Laurence-Moon-Biedl syndrome until BARDET-BIEDL SYNDROME was identified as a distinct entity.[bioportfolio.com] Laurence-moon Syndrome An autosomal recessive condition characterized by hypogonadism; spinocerebellar degeneration; MENTAL RETARDATION; RETINITIS PIGMENTOSA; and OBESITY.[bioportfolio.com]

  • Ichthyosis-Intellectual Disability-Dwarfism-Renal Impairment Syndrome

    Neuropathy target esterase impairments cause Oliver-McFarlane and Laurence-Moon syndromes. J. Med. Genet. 2015;(52): 85-94. Scheidecker S, Etard C, Pierce NW, et al.[rarediseases.org] Bardet-Biedl syndrome: Genetics, molecular pathophysiology, and disease management. Indian J Ophthalmol. 2016;64(9): 620-627. Hufnagel RB, Arno G, Hein ND, et al.[rarediseases.org]

  • 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] 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] […] hypomyelinating leukodystrophy) IBA57 * SPG74 KDM5C MRXSCJ X-linked Intellectual disability, Claes-Jensen type KIF1A SPG30 KIF1C SPAX2 spastic ataxia 2 KIF5A SPG10 L1CAM SPG11 L1 syndrome[invitae.com]

Further symptoms