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5,073 Possible Causes for Mental Retardation (15%)

Did you mean: Mental Retardation, (15%)

  • Mental Retardation

    […] another possible cause of mental retardation.[web.archive.org] […] syndromic intellectual disability MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15 slowness IQ under 70 intelligence quotient under 70 Intellectual Disabilities rare intellectual[wikidata.org] American Association on Mental Retardation. Mental retardation. Definition, classification and systems of supports. 9th ed. Washington, D.C.: the Association, 1993.[web.archive.org]

  • X-Linked Intellectual Disability-Psychosis-Macroorchidism Syndrome

    An X-linked recessive basal ganglia disorder with mental retardation.[ncbi.nlm.nih.gov] (DO) Synonyms: exact_synonym: Lindsay-Burn syndrome; MRX16; MRX79; MRXS13; PPM-X; PPMX; X-linked mental retardation 16; X-linked mental retardation 79; X-linked mental retardation[rgd.mcw.edu] […] deficit, X-linked - psychosis - macroorchidism; Mental retardation psychosis macroorchidism; Mental retardation, X-linked, syndromic 13; MRXS13; Mental retardation with psychosis[rarediseases.info.nih.gov]

  • Dyggve-Melchior-Clausen Syndrome

    Continuing studies will help to decide whether Smith-McCort syndrome, which causes the same skeletal manifestations but no mental retardation, 15 also maps to this region.[jmg.bmj.com] Abstract The Dyggve-Melchior-Clausen syndrome is an inherited disorder of skeletal development characterized by short-trunked dwarfism, mental retardation, and a distinctive[ncbi.nlm.nih.gov] Identifying the DMC gene will hopefully help to elucidate the pathogenesis of this poorly understood bone dysplasia-mental retardation syndrome.[jmg.bmj.com]

  • Impacted Cerumen

    Moreover, a strong propensity for recurrent cerumen impaction in the mentally retarded population was found.[ncbi.nlm.nih.gov] Abstract The incidence of occlusion of the external auditory canal due to impacted cerumen was determined for 44 mentally retarded subjects in comparison with 44 nonretarded[ncbi.nlm.nih.gov] Impacted cerumen is a major cause of primary care consultation, and a common comorbidity in ENT patients, the elderly, infirm and people with mental retardation.[ncbi.nlm.nih.gov]

  • Patau Syndrome

    Survivors suffer from severe mental retardation and health problems all their lives.[symptoma.com] It leads to a variety of abnormalities that include mental retardation, microcephaly, low-set ears, eye structural defects, polydactyly, and limb abnormalities The presence[icd9data.com] retardation may complicate survival Please rate topic.[medbullets.com]

  • Sjogren-Larsson Syndrome

    When ichthyosis is associated with spasticity and mental retardation, one should consider SLS.[ncbi.nlm.nih.gov] His quadriplegia was managed by aggressive physiotherapy and mental retardation by stimulation techniques.[ncbi.nlm.nih.gov] Sjögren-Larsson syndrome is an autosomal-recessive hereditary disorder involving congenital ichthyosis, mental retardation, and spastic diplegia or tetraplegia.[ncbi.nlm.nih.gov]

  • Acrocallosal Syndrome

    […] characterized by corpus callosum agenesis, polydactyly, multiple dysmorphic features, motor and mental retardation ACLS SCHINZEL ACROCALLOSAL SYNDROME Schinzel syndrome 1[wikidata.org] retardation.[ncbi.nlm.nih.gov] Jump to search syndrome that is an autosomal recessive disorder, which is characterized by corpus callosum agenesis, polydactyly, multiple dysmorphic features, motor and mental[wikidata.org]

  • Smith Lemli Opitz Syndrome

    This article attempts to describe a very unusual case of a boy aged 15, who has had intractable epileptic phenomena, mental retardation, megalocephaly, micrognathy, syndactyly[ncbi.nlm.nih.gov] It comprises a characteristic combination of facial features, malformations, and mental retardation.[ncbi.nlm.nih.gov] retardation syndromes.[ncbi.nlm.nih.gov]

  • Mowat-Wilson Syndrome

    The mental retardation, usually severe, was constant; the delay in the acquisition of motor skills was more variable (table 2).[jmg.bmjjournals.com] The genotype-phenotype analysis confirmed that ZFHX1B deletions and mutations result in a recognizable facial dysmorphism with a multiple congenital anomaly and mental retardation[ncbi.nlm.nih.gov] Late infantile Hirschsprung disease-mental retardation syndrome with a 3-bp deletion in ZFHX1B. Neurology 2002 ; 59 : 1637 –40.[jmg.bmjjournals.com]

  • Oculocerebrorenal Syndrome

    […] skills than means of either populations of individuals with mental retardation or visual impairment.[ncbi.nlm.nih.gov] Clinical manifestations include congenital cataract, mental retardation, and renal tubular dysfunction.[ncbi.nlm.nih.gov] MacLachlan: Organic aciduria, decreased renal ammoniac production, hydrophthalmos, and mental retardation. A distinct clinical entity.[whonamedit.com]

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