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Sjögrenov-Larssonov syndróm

  1. Subject h.Sjögrenov-Larssonov syndróm
    Subject h.Sjogren-Larsson Syndrome
    Entry termssyndroma Rud
    Scope note in EnglishAn autosomal recessive neurocutaneous disorder characterized by severe ichthyosis MENTAL RETARDATION; SPASTIC PARAPLEGIA; and congenital ICHTHYOSIS. It is caused by mutation of gene encoding microsomal fatty ALDEHYDE DEHYDROGENASE leading to defect in fatty alcohol metabolism.
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Number of the records: 1  

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