Proximal tubulopathy - diabetes mellitus - cerebellar ataxia (Q102278): Difference between revisions

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A síndrome Tubulopatia proximal - diabetes mellitus - ataxia cerebelar é caracterizada pelo aparecimento de tubulopatia proximal no primeiro ano de vida, seguido por desenvolvimento progressivo de anomalias cutâneas durante a infância (eritrocianose e pigmentação anormal), deficiência visual , osteoporose, ataxia cerebelar, miopatia mitocondrial, surdez e diabetes mellitus.
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Proximal tubulopathy - diabetes mellitus - cerebellar ataxia syndrome is characterised by onset of proximal tubulopathy in the first year of life, followed by progressive development during childhood of skin anomalies (erythrocyanosis and abnormal pigmentation), blindness, osteoporosis, cerebellar ataxia, mitochondrial myopathy, deafness and diabetes mellitus.

Revision as of 19:12, 16 August 2026

Proximal tubulopathy - diabetes mellitus - cerebellar ataxia syndrome is characterised by onset of proximal tubulopathy in the first year of life, followed by progressive development during childhood of skin anomalies (erythrocyanosis and abnormal pigmentation), blindness, osteoporosis, cerebellar ataxia, mitochondrial myopathy, deafness and diabetes mellitus.
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    Proximal tubulopathy - diabetes mellitus - cerebellar ataxia
    Proximal tubulopathy - diabetes mellitus - cerebellar ataxia syndrome is characterised by onset of proximal tubulopathy in the first year of life, followed by progressive development during childhood of skin anomalies (erythrocyanosis and abnormal pigmentation), blindness, osteoporosis, cerebellar ataxia, mitochondrial myopathy, deafness and diabetes mellitus.

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