Literature DB >> 16272804

Long-acting gonadotropin-releasing hormone analogue treatment for central precocious puberty in maternal uniparental disomy chromosome 14.

Ikuko Takahashi1, Tsutomu Takahashi, Maki Utsunomiya, Goro Takada, Akio Koizumi.   

Abstract

Uniparental disomy (UPD) is the inheritance of a chromosome pair from one parent and is increasingly recognized as a cause of abnormal phenotypes either due to imprinted genes or, in the case of isodisomy, to homozygosity of recessive alleles. Maternal uniparental disomy for chromosome 14 (matUPD[14]) may cause a characteristic phenotype including precocious puberty. Central precocious puberty (CPP) was diagnosed in a 6-year-old girl with some dysmorphic features, truncal obesity, small hands, and small feet. Cytogenetic analysis of her peripheral blood demonstrated chromosomal rearrangement: Robertsonian translocation 45, XX, der(13;14)(q10;q10). MatUPD(14) was demonstrated in the patient by haplotype analysis of chromosome 14, showing that the CPP is one of the features caused by matUPD(14). The CPP was successfully treated with higher dosage of long-acting gonadotropin releasing hormone (GnRH) analogue, Leuprolide, 90 microg/kg/month. This is the first report that describes GnRH analogue treatment for CPP associated with matUPD(14), suggesting that the GnRH analogue treatment is appropriate even for such a specific type of CPP.

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Year:  2005        PMID: 16272804     DOI: 10.1620/tjem.207.333

Source DB:  PubMed          Journal:  Tohoku J Exp Med        ISSN: 0040-8727            Impact factor:   1.848


  4 in total

1.  Growth parameters in maternal uniparental disomy 7 and 14.

Authors:  Dieter Kotzot
Journal:  Eur J Pediatr       Date:  2007-01-04       Impact factor: 3.183

2.  Maternal uniparental disomy of the chromosome 14: need for growth hormone provocative tests also when a deficiency is not suspected.

Authors:  Anna Tortora; Domenico La Sala; Fortunato Lonardo; Mario Vitale
Journal:  BMJ Case Rep       Date:  2019-05-10

3.  Maternal uniparental disomy 14 and mosaic trisomy 14 in a Chinese boy with moderate to severe intellectual disability.

Authors:  Shujie Zhang; Haisong Qin; Jin Wang; Luping OuYang; Shiyu Luo; Chunyun Fu; Xin Fan; Jiasun Su; Rongyu Chen; Bobo Xie; Xuyun Hu; Shaoke Chen; Yiping Shen
Journal:  Mol Cytogenet       Date:  2016-08-24       Impact factor: 2.009

Review 4.  The tempo of human childhood: a maternal foot on the accelerator, a paternal foot on the brake.

Authors:  Jennifer Kotler; David Haig
Journal:  Evol Anthropol       Date:  2018-03-25
  4 in total

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