Literature DB >> 17916866

One-year-old male with accelerated growth and development.

Ajit Singh Kashyap1, Kuldip Parkash Anand, Surekha Kashyap, Sumeet Arora.   

Abstract

A 1-year-old male child with isosexual central (gonadotropin-dependent) precocious puberty caused by hypothalamic hamartoma is reported. Details of the diagnosis based solely on neuromaging characteristics, and satisfactory results of medical treatment with gonadotropin releasing hormone agonist analogues, are highlighted.

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Year:  2007        PMID： 17916866      PMCID： PMC2600118          DOI： 10.1136/pgmj.2007.062307

Source DB:  PubMed          Journal:  Postgrad Med J        ISSN： 0032-5473            Impact factor:   2.401


  4 in total

1.  Treatment of gonadotropin dependent precocious puberty due to hypothalamic hamartoma with gonadotropin releasing hormone agonist depot.

Authors:  V N de Brito; A C Latronico; I J Arnhold; L S Lo; S Domenice; M C Albano; M C Fragoso; B B Mendonca
Journal:  Arch Dis Child       Date:  1999-03       Impact factor: 3.791

2.  The luteinizing hormone-releasing hormone-secreting hypothalamic hamartoma is a congenital malformation: natural history.

Authors:  P Mahachoklertwattana; S L Kaplan; M M Grumbach
Journal:  J Clin Endocrinol Metab       Date:  1993-07       Impact factor: 5.958

3.  Hamartomas of the tuber cinereum: CT, MR, and pathologic findings.

Authors:  O B Boyko; J T Curnes; W J Oakes; P C Burger
Journal:  AJNR Am J Neuroradiol       Date:  1991 Mar-Apr       Impact factor: 3.825

4.  MR imaging and spectroscopic study of epileptogenic hypothalamic hamartomas: analysis of 72 cases.

Authors:  Jeremy L Freeman; Lee T Coleman; R Mark Wellard; Michael J Kean; Jeffrey V Rosenfeld; Graeme D Jackson; Samuel F Berkovic; A Simon Harvey
Journal:  AJNR Am J Neuroradiol       Date:  2004-03       Impact factor: 3.825
  4 in total

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