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pseudohypoparatyreóza

  1. Subject h.pseudohypoparatyreóza
    Subject h.Pseudohypoparathyroidism
    Entry termsAlbrightova dedičná osteodystrofia
    Albrightova hereditárna osteodystrofia
    Albrightova hereditárna osteodystrofia s mnohonásobnou hormonálnou rezistenciou
    pseudohypoparatyreoidizmus
    PHPIa
    PHP Ia
    PHD1b
    PHD Ib
    English X referencesAlbright Hereditary Osteodystrophy
    PHPIa
    Scope note in EnglishA hereditary syndrome clinically similar to HYPOPARATHYROIDISM. It is characterized by HYPOCALCEMIA; HYPERPHOSPHATEMIA; and associated skeletal development impairment and caused by failure of response to PARATHYROID HORMONE rather than deficiencies. A severe form with resistance to multiple hormones is referred to as Type 1a and is associated with maternal mutant allele of the ALPHA CHAIN OF STIMULATORY G PROTEIN.
    See also reference (FX) in Slovak alfa podjednotky proteínu viažuceho GTP, Gs
    See also reference (FX) in English GTP-Binding Protein alpha Subunits, Gs
    Links (5) - ARTICLES
    (1) - MeSH descriptor
    (1) - CiBaMed
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Number of the records: 1  

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