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      Long-term growth hormone therapy in mitochondrial cytopathy.

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          Abstract

          To describe in a 5-year-old Caucasian male with mitochondrial cytopathy, a biochemical growth hormone (GH) deficiency associated with normal GH biological activity as evaluated by Nb2 cell bioassay and normal serum IGF-I and IGFBP3 values increasing slightly after GH administration.

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          Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

          W Reardon, M.E. Pembrey, R.C. Trembath … (1992)
          Article 0 comments Cited 14 times – based on 0 reviews     Review now
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            Kearns-Sayre syndrome. A review of a multisystem disorder of children and young adults.

            I Butler, N. Gadoth (1976)
            The syndrome of a slowly progressive external ophthalmoplegia, pigment retinopathy, and disorder of cardiac conduction was described by Kearns and Sayre in 1958. In patients with this triad, other neurological deficits may occur with associated abnormalities of the electrocardiogram, electroencephalogram, audiogram, and an elevation of protein in cerebrospinal fluid. The onset of a potentially lethal cardiac dysrhythmia in a patient with this slowly progressive degeneration of the nervous system can be anticipated and prevented by the use of an artivicial cardiac pacemaker.
            Article 0 comments Cited 2 times – based on 0 reviews     Review now
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              Author and article information

              Journal
              Journal ID (iso-abbrev): Horm. Res.
              Title: Hormone research
              Publisher: S. Karger AG
              ISSN: 0301-0163
              ISSN (Print): 0301-0163
              Publication date (Electronic): 2004
              Volume: 62
              Issue: 2
              Affiliations
              [1 ] Department of Pediatrics, University of Pavia, IRCCS San Matteo, Pavia, Italy. salvatorebarberi@hotmail.com
              Article
              Publisher Item ID: 80451
              DOI: 10.1159/000080451
              PubMed ID: 15331853
              SO-VID: 289c37f1-7cb5-49f0-be63-0ba0ad58b625
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