Literature DB >> 8821908

Precocious puberty in three boys with Sanfilippo A (mucopolysaccharidosis III A).

A Tylki-Szymańska1, M Metera.   

Abstract

Three boys with mucopolysaccharidosis type III A (Sanfilippo) entered puberty at the ages of 5.9, 6.6 and 9.6 years. The diagnosis of central precocious puberty (GnRH-dependent) was established on the basis of pubertal levels of basal and GnRH-stimulated gonadotropins, LH and FSH. All the patients were tall from early infancy, but there was no acceleration of growth velocity or bone maturation despite advanced pubertal stage and high testosterone levels. Computerized tomography of the brain showed changes which are characteristic for Sanfilippo. This is the first time that precocious puberty has been described in Sanfilippo patients. The question of whether the precocious puberty in our Sanfilippo patients is a coincidence or is related in some way remains open.

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Year:  1995        PMID: 8821908     DOI: 10.1515/jpem.1995.8.4.291

Source DB:  PubMed          Journal:  J Pediatr Endocrinol Metab        ISSN: 0334-018X            Impact factor:   1.634


  4 in total

1.  Growth patterns and the use of growth hormone in the mucopolysaccharidoses.

Authors:  L E Polgreen; B S Miller
Journal:  J Pediatr Rehabil Med       Date:  2010

2.  Precocious initiation of spermatogenesis in a 19-month-old boy with Hurler syndrome.

Authors:  Jean-Pierre Milazzo; Amandine Bironneau; Jean-Pierre Vannier; Agnes Liard-Zmuda; Bertrand Macé; Rives Nathalie
Journal:  Basic Clin Androl       Date:  2014-05-01

3.  Central Precocious Puberty in a Child With Metachromatic Leukodystrophy.

Authors:  Gilda Belli; Emanuele Bartolini; Andrea Bianchi; Mario Mascalchi; Stefano Stagi
Journal:  Front Endocrinol (Lausanne)       Date:  2018-08-24       Impact factor: 5.555

4.  Growth charts for patients with Sanfilippo syndrome (Mucopolysaccharidosis type III).

Authors:  Nicole M Muschol; Daniel Pape; Kai Kossow; Kurt Ullrich; Laila Arash-Kaps; Julia B Hennermann; Ralf Stücker; Sandra R Breyer
Journal:  Orphanet J Rare Dis       Date:  2019-05-02       Impact factor: 4.123

  4 in total

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