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Cerebroatrophic hyperammonemia symptoms, causes, diagnosis, and treatment information for Cerebroatrophic hyperammonemia (Rett's syndrome) with alternative diagnoses, full-text book chapters, misdiagnosis, research treatments, prevention, and prognosis. ... Description of Cerebroatrophic hyperammonemia...
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Rett's syndrome: Autism-like behavioral syndrome in infant girls. ... Rett Syndrome, cerebroatrophic hyperammonemia, Autism, dementia, ataxia, and loss of purposeful hand use, RTT, RTS ... Cerebroatrophic hyperammonemia Source - Diseases Database;
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Rett syndrome - Wikipedia, the free encyclopedia
Rett syndrome is a neurodevelopmental disorder that is classified as an autism spectrum disorder by the DSM-IV. It was first described by Austrian pediatrician Andreas Rett in 1966. The clinical feat...
en.wikipedia.org/wiki/Rett_syndrome |
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Rett syndrome is a disorder of brain development that occurs almost exclusively in girls. After 6 to 18 months of apparently ... hyperammonemia ; inheritance ; microcephaly ; mutation ; nerve cell ; new mutation ; pattern of inheritance ; protein ; scoliosis ; seizure ; sex chromosomes ; sign ; spectrum ; symptom ;
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: Rett's Disorder; Syndrome, Rett; Rett's Syndrome; Autism Dementia Ataxia Loss of Purposeful Hand Use Syndrome; Cerebroatrophic Hyperammonemia Show All >>;
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Ultrasonographic findings in dogs with hyperammonemia: 90 cases ...; OBJECTIVE: To determine ultrasonographic abnormalities in dogs with hyperammonemia. DESIGN: Retrospective study. ANIMALS: 90 client-owned dogs with ;
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Cerebroatrophic Hyperammonemia, Autism-Dementia-Ataxia-Loss of Purposeful Hand Use Syndrome, Rett Disorder, RS ... Cerebroatrophic Hyperammonemia +, Autism-Dementia-Ataxia-Loss of Purposeful Hand Use Syndrome +, Rett Disorder +, and RS +
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ammoniemia; arginase deficiency; arginine; cerebroatrophic hyperammonemia; explosive syndrome; HHH syndrome; homocitrullinuria; hyperammoniemia; hyperammonuria; hyperlysinuria with hyperammonemia;
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Synonyms and related keywords: pervasive developmental disorder, PDD, Rett syndrome, RS, cerebroatrophic hyperammonemia, neurologic disorder, neurodevelopmental arrest, genetic disorder, severe congenital encephalopathy, dystonia apraxia, retardation, epilepsy, oral-motor dysfunction,
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