Literature DB >> 34539919

Growth Hormone Dynamics among Children with Mixed Gonadal Dysgenesis (45,X/46,XY).

D Das1.   

Abstract

CONTEXT: Learn the growth hormone dynamics and discuss the issues of growth hormone therapy in subjects with 45,X/46XY.
OBJECTIVE: To study the growth hormone dynamics in children with 45,X/46,XY karyotyping and mixed gonadal dysgenesis (MGD).
DESIGN: Descriptive clinical study. PARTICIPANTS: Five subjects with karyotype 45,X / 46,XY with or without genital ambiguity and somatic features of SHOX haploinsufficiency.
INTERVENTIONS: Growth hormone dynamic study and gonadectomy. MAIN OUTCOME: IGF-1, peak GH levels, Turner's stigmata and histology of gonadal tissue.
RESULTS: Five cases of MGD with both male and female phenotype were studies. IGF-1 levels and GH levels showed both features of growth hormone deficiency and growth hormone insensitivity. One study subject has gonadal germ cell tumour (dysgerminoma). We discuss here the issues regarding the GH therapy in MGD subjects.
CONCLUSION: Growth deceleration in MGD subjects is partly due to defective growth hormone secretion and partly due to growth hormone insensitivity. MGD subjects are at high risk for occurrence of gonadal tumours. Gonadectomy or biopsy of underlying dysgenetic gonads is essential prior GH therapy. Close surveillance for second neoplasm is to be considered in subjects with history of gonadal tumors prior starting GH for short stature. ©by Acta Endocrinologica Foundation.

Entities:  

Keywords:  Gonadal Germ cell tumours; Growth hormone; Mixed gonadal dysgenesis; Second neoplasm

Year:  2021        PMID: 34539919      PMCID: PMC8417479          DOI: 10.4183/aeb.2021.117

Source DB:  PubMed          Journal:  Acta Endocrinol (Buchar)        ISSN: 1841-0987            Impact factor:   1.104


  20 in total

1.  Reduced free IGF-I and increased IGFBP-3 proteolysis in Turner syndrome: modulation by female sex steroids.

Authors:  C H Gravholt; J Frystyk; A Flyvbjerg; H Orskov; J S Christiansen
Journal:  Am J Physiol Endocrinol Metab       Date:  2001-02       Impact factor: 4.310

Review 2.  Germ cell tumors in the intersex gonad: old paths, new directions, moving frontiers.

Authors:  Martine Cools; Stenvert L S Drop; Katja P Wolffenbuttel; J Wolter Oosterhuis; Leendert H J Looijenga
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Review 3.  Growth hormone treatment in non-growth hormone-deficient children.

Authors:  Sandro Loche; Luisanna Carta; Anastasia Ibba; Chiara Guzzetti
Journal:  Ann Pediatr Endocrinol Metab       Date:  2014-03-31

4.  The role of a clinical score in the assessment of ambiguous genitalia.

Authors:  S F Ahmed; O Khwaja; I A Hughes
Journal:  BJU Int       Date:  2000-01       Impact factor: 5.588

5.  Adult growth hormone replacement therapy and neuroimaging surveillance in brain tumour survivors.

Authors:  Andreas Jostel; Annice Mukherjee; Paul A Hulse; Stephen M Shalet
Journal:  Clin Endocrinol (Oxf)       Date:  2005-06       Impact factor: 3.478

6.  The sitting height/height ratio for age in healthy and short individuals and its potential role in selecting short children for SHOX analysis.

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7.  SHOX haploinsufficiency and Leri-Weill dyschondrosteosis: prevalence and growth failure in relation to mutation, sex, and degree of wrist deformity.

Authors:  Gerhard Binder; Alexandra Renz; Alicia Martinez; Ana Keselman; Volker Hesse; Stefan W Riedl; Gabriele Häusler; Susanne Fricke-Otto; Herwig Frisch; Juan Jorge Heinrich; Michael B Ranke
Journal:  J Clin Endocrinol Metab       Date:  2004-09       Impact factor: 5.958

8.  Short stature in a phenotypic male caused by mixed gonadal dysgenesis.

Authors:  Christina M Jacobsen; Laurie E Cohen
Journal:  Nat Clin Pract Endocrinol Metab       Date:  2008-07-22

9.  Phenotypic spectrum of 45,X/46,XY males with a ring Y chromosome and bilaterally descended testes.

Authors:  Lawrence C Layman; Sandra P T Tho; Andrew D Clark; Anita Kulharya; Paul G McDonough
Journal:  Fertil Steril       Date:  2008-06-16       Impact factor: 7.329

10.  Short stature in children with an apparently normal male phenotype can be caused by 45,X/46,XY mosaicism and is susceptible to growth hormone treatment.

Authors:  Annette Richter-Unruh; Sabine Knauer-Fischer; Stefan Kaspers; Beate Albrecht; Gabriele Gillessen-Kaesbach; Berthold P Hauffa
Journal:  Eur J Pediatr       Date:  2004-02-18       Impact factor: 3.183

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