Literature DB >> 20411478

Intrauterine growth retardation associated with precocious puberty and sertoli cell hyperplasia.

M B Lodish1, L A Gartner, P Albini, G Sabnis, A Brodie, J M Meck, A M Meloni-Ehrig, S Hill, E Tsilou, V A Valera, B A Walter, M J Merino, C A Stratakis.   

Abstract

The original description of patients with Russell-Silver syndrome included precocious puberty, the mechanism of which was unclear. We describe a child with a Russell-Silver syndrome-like phenotype who presented with precocious puberty that was associated with hyperplasia of the Sertoli cells. The patient was found to have an immature cryptorchid testicle; hyperplastic Sertoli cells were also aneuploid carrying trisomy 8. This chromosomal abnormality was present in Sertoli cells only and could not be detected in peripheral lymphocytes, tunica vaginalis, or other, normal, testicular tissue. Sertoli cells in culture showed excess aromatization providing an explanation for the rapid advancement of the patient's bone age. We conclude that in a patient with a Russell-Silver syndrome-like phenotype, Sertoli cell hyperplasia was associated with somatic trisomy 8, increased aromatization, and gonadotropin-independent precocious puberty. Copyright Georg Thieme Verlag KG Stuttgart New York.

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Year:  2010        PMID: 20411478      PMCID: PMC3412584          DOI: 10.1055/s-0030-1252021

Source DB:  PubMed          Journal:  Horm Metab Res        ISSN: 0018-5043            Impact factor:   2.936


  32 in total

Review 1.  The genetic aetiology of Silver-Russell syndrome.

Authors:  S Abu-Amero; D Monk; J Frost; M Preece; P Stanier; G E Moore
Journal:  J Med Genet       Date:  2007-12-21       Impact factor: 6.318

2.  Reevaluation of Russell-Silver syndrome.

Authors:  H M Saal; R A Pagon; M G Pepin
Journal:  J Pediatr       Date:  1985-11       Impact factor: 4.406

3.  Chromosome 2 (2p16) abnormalities in Carney complex tumours.

Authors:  L Matyakhina; S Pack; L S Kirschner; E Pak; P Mannan; J Jaikumar; S E Taymans; F Sandrini; J A Carney; C A Stratakis
Journal:  J Med Genet       Date:  2003-04       Impact factor: 6.318

4.  The spectrum of Silver-Russell syndrome: a clinical and molecular genetic study and new diagnostic criteria.

Authors:  S M Price; R Stanhope; C Garrett; M A Preece; R C Trembath
Journal:  J Med Genet       Date:  1999-11       Impact factor: 6.318

5.  Aromatase expression in the human male.

Authors:  A Brodie; S Inkster; W Yue
Journal:  Mol Cell Endocrinol       Date:  2001-06-10       Impact factor: 4.102

Review 6.  Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases.

Authors:  Emanuela Maserati; Fiorenza Aprili; Fabrizio Vinante; Franco Locatelli; Giovanni Amendola; Adriana Zatterale; Giuseppe Milone; Antonella Minelli; Franca Bernardi; Francesco Lo Curto; Francesco Pasquali
Journal:  Genes Chromosomes Cancer       Date:  2002-01       Impact factor: 5.006

7.  Bilateral cystic nephroblastomas and multiple malformations with trisomy 8 mosaicism.

Authors:  Y Nakamura; H Nakashima; S Fukuda; T Hashimoto; M Maruyama
Journal:  Hum Pathol       Date:  1985-07       Impact factor: 3.466

8.  Comparison of single versus multiple dose regimens for the human chorionic gonadotropin stimulatory test.

Authors:  T F Kolon; O F Miller
Journal:  J Urol       Date:  2001-10       Impact factor: 7.450

9.  Trisomy 8 mosaicism syndrome. Two cases demonstrating variability in phenotype.

Authors:  Z E Kurtyka; B Krzykwa; E Piatkowska; M Radwan; J J Pietrzyk
Journal:  Clin Pediatr (Phila)       Date:  1988-11       Impact factor: 1.168

10.  Diploid-triploid mixoploidy: clinical and cytogenetic aspects.

Authors:  J M Graham; H Hoehn; M S Lin; D W Smith
Journal:  Pediatrics       Date:  1981-07       Impact factor: 7.124

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  1 in total

Review 1.  The evolutionary biology of child health.

Authors:  Bernard Crespi
Journal:  Proc Biol Sci       Date:  2011-02-02       Impact factor: 5.349

  1 in total

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