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1,247 Possible Causes for Pediatric Disorder, Severe Mental Retardation in Some Patients

Did you mean: Pediatric Disorder, Severe Mental Retardation, in Some Patients

  • Patau Syndrome

    Survivors suffer from severe mental retardation and health problems all their lives.[] Nelson Textbook of Pediatrics. 20th ed. Philadelphia, PA: Elsevier; 2016:chap 81. Madan-Khetapal S, Arnold G. Genetic disorders and dysmorphic conditions.[] mental retardation may complicate survival Please rate topic.[]

  • Phenylketonuria

    Untreated patients usually exhibit severe mental retardation and poor motor function, with characteristic T2 white matter signal abnormalities on conventional MR images.[] Author information 1 Medical and Rehabilitation Centre in Gdansk, Gdansk, Poland. 2 Department of Pediatrics and Developmental Disorders of Children and Adolescents, Medical[] Clinical findings included hair hypopigmentation, microcephaly, severe mental retardation with absent development of verbal language and autistic symptoms in all three patients[]

  • Klinefelter Syndrome

    In these individuals, the classic features of Klinefelter syndrome may be exaggerated, with low I.Q. or moderate to severe mental retardation also occurring.[] disorders, resulting in a rise in the diagnosis and early referral to the pediatric endocrinologist.[] Nearly all patients were severely mentally retarded, with IQ levels usually ranging from 20 to 60. 96 In contrast to 47,XXY patients, 49,XXXXY patients often exhibit micropenis[]

  • Autism

    We report an 18-year-old female with a diagnosis of DSM-IV Autistic Disorder and moderate to severe mental retardation who was discovered to have a previously undescribed[] In two, randomized, double-blind, placebo-controlled studies in pediatric patients aged 6-17 years with irritability associated with autistic disorder, 8 weeks of treatment[] Abstract A boy with autistic disorder and severe mental retardation developed severe dyskinesias, including objective akathisia (probable) and tics, a month after discontinuation[]

  • Aspartylglucosaminuria

    Abstract Aspartylglucosaminuria (AGU) is a lysosomal storage disease resulting in severe mental retardation.[] Disorders E-2903 168 Measurement of Health Outcomes in Pediatric Neurologic Disorders E-2910 169 The Influence of Computer Resources on Child Neurology E-2918 170 Education[] The activity of this lysosomal enzyme is deficient in aspartylglucosaminuria (AGU), a recessively inherited lysosomal accumulation disease resulting in severe mental retardation[]

  • Aicardi's Syndrome

    Children with Aicardi syndrome have moderate to severe mental retardation and difficult to control fits.[] ., Shevell, M.I. (1998) Infantile epileptic encephalopathy (Ohtahara syndrome) and migrational disorder.[] Nelson Textbook of Pediatrics. 20th ed. Philadelphia, PA: Elsevier; 2016:chap 591. Samat HB, Flores-Samat L. Developmental disorders of the nervous system.[]

  • Mucopolysaccharidosis 1H

    mental retardation.[] Pediatrics. 1999;103(6):1158–66. View Article PubMed Google Scholar Manikam R, Perman JA. Pediatric feeding disorders. J Clin Gastroenterol. 2000;30(1):34–46.[] The mucopolysaccharidoses: a heterogeneous group of disorders with variable pediatric presentations. J Pediatr. 2004 May;144(5 Suppl):S27-34. Review.[]

  • Rett Syndrome

    mental retardation (MR) in whom the most common forms of MR have been excluded.[] El-Bitar, Degenerative Disorders Primarily of Gray Matter, Swaiman's Pediatric Neurology, 10.1016/B978-1-4377-0435-8.00041-X, (518-543), (2012). Eveline E. O.[] RTT clinical expression is typically characterized by loss of purposeful hand movements, severe mental retardation and motor impairment, breathing disorders, ataxia and increased[]

  • Pyridoxine Dependency Syndrome

    Pyridoxine-dependent seizures can be associated with autism, breath holding and severe mental retardation(2).[] The pediatric neurotransmitter disorders. J Child Neurol. 2007 May;22(5):606-16. Review.[] Pediatr Neurol. 2006; 34 :164–7. [ PubMed : 16458834 ] Ohtsuka Y, Hattori J, Ishida T, Ogino T, Oka E.[]

  • Cerebro-Oculo-Facio-Skeletal Syndrome

    We report a 14-year-old male, born to consanguineous parents, with microcephaly, intracranial calcification, severe mental retardation, cataracts, optic atrophy, pigmentary[] Cerebro-oculo-facio-skeletal syndrome (COFS) is a pediatric, genetic, degenerative disorder that involves the brain and the spinal cord.[] Cerebro-oculo-facio-skeletal (COFS) syndrome is a rare autosomal-recessive disorder that includes microcephaly, severe mental retardation, and multiple congenital anomalies[]

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