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24 Possible Causes for Hyporeflexia (Later), Speech and Language Abnormalities

Did you mean: Hyporeflexia (Later, Speech and Language Abnormalities

  • Motor Neuron Disease

    , hyperreflexia and atrophy in later stages of disease, but fasciculations are absent.[] In the setting of LMN damage, hyporeflexia, atrophy, decreased muscle tone and fasciculations develop, while diseases that affect UMNs cause spasticity, increased muscle tone[]

  • Autosomal Recessive Spastic Paraplegia Type 26

    […] jaw, and speech and language disorders.[] Phenotypic abnormalities associated with Fragile X syndrome include developmental delay/intellectually disability, autistic behaviors, characteristic narrow face with large[]

  • Cerebral Palsy

    Adrenoleukodystrophy begins later in childhood, but other leukodystrophies begin earlier and may be mistaken for CP at first.[] Because children with CP may have associated deficits of mental retardation, ophthalmologic and hearing impairments, speech and language disorders, and oral-motor dysfunction[] While many of these children understand language, their ability to produce speech may be affected.[]

  • Glycogen Storage Disease due to Phosphoglycerate Mutase Deficiency

    Abnormality of cardiovascular system morphology Delayed speech and language development Malar flattening Long philtrum Short nose Hypertonia Atrial septal defect Tremor Ventricular[] Muscle atrophy appears early and is accompanied by hyporeflexia.[] […] concentration Capsular cataract Peripheral visual field loss Menstrual irregularities Epicanthus Feeding difficulties Insulin-resistant diabetes mellitus Arrhythmia Absent speech[]

  • Oculomotor Apraxia

    The upper limbs are involved somewhat later but with less pronounced movement impairment. Hyporeflexia or areflexia is common.[] Vinck A, Verhagen MM, Gerven Mv, de Groot IJ, Weemaes CM, et al. (2011) Cognitive and speech-language performance in children with ataxia telangiectasia.Dev Neurorehabil 14[] Failure to thrive, marked psychomotor retardation, delayed development, growth retardation, and ataxia become evident later in those who survive.[]

  • Autosomal Recessive Spastic Paraplegia Type 18

    (AHC) Later - CST involvement with brisk reflexes in the legs, spasticity, and weakness May occur as a late sequelae to trauma Can see in association with Arnold Chiari malformation[] Absent speech development Lack of language development Lack of speech No speech development No speech or language development Nonverbal [ more ] 0001344 Autosomal recessive[] Cervical cord most common site Loss of pain and temperature related to the crossing fibers occurs early cape like sensory loss Weakness of muscles in arms with atrophy and hyporeflexia[]

  • Autosomal Recessive Spinocerebellar Ataxia Type 17

    […] jaw, and speech and language disorders.[] SCA2 differs clinically from other types of SCAs because of the slow saccade and hyporeflexia [ 22 ].[] Phenotypic abnormalities associated with Fragile X syndrome include developmental delay/intellectually disability, autistic behaviors, characteristic narrow face with large[]

  • Abetalipoproteinemia

    , myopathy, retinitis pigmentosa, peripheral neuropathy, hyporeflexia and ataxia.[] Dysarthria Speech & language therapy W/early vitamin E supplementation dysarthria is rare.[] Eyes : Retinitis Pigmentosa, blindness in later stages (if untreated). Hematologic : Acanthocytosis (abnormal shaped RBCs), Hemolytic anemia.[]

  • Transcobalamin 2 Deficiency

    An abnormally small head. Intellectual disabilities, lower IQ. Language delay or speech problems. Poor motor and coordination skills. Poor socialization.[] In early stages, decreased position and vibratory sensation in the extremities is accompanied by mild to moderate weakness and hyporeflexia.[] In later stages, spasticity, extensor plantar responses, greater loss of position and vibratory sensation in the lower extremities, and ataxia emerge.[]

  • Autosomal Dominant Myoglobinuria

    Symptoms: ataxia, sensory loss and hyporeflexia chiefly in lower extremities; later nystagmus and dysarthria; onset in childhood and adolescence; autosomal recessive. h.[] […] movements, loss of speech, and seizures 1 Neurodevelopmental disorder with severe motor impairment and absent language 1 Neurodevelopmental disorder with spasticity and poor[] Lower motor neuron symptoms: muscle atrophy, fasciculations, hyporeflexia, dysphagia.[]

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