Gonadotrophin-independent precocious puberty and dyschondrosteosis

Leena Patel; Peter E. Clayton; Maurice Super; David A. Price

doi:10.1515/JPEM.1994.7.3.265

Gonadotrophin-independent precocious puberty and dyschondrosteosis

Leena Patel
, Peter E. Clayton
, Maurice Super
, David A. Price^*

^*Corresponding author for this work

Royal Manchester Children's Hospital

Research output: Contribution to journal › Article › peer-review

Abstract

We present a case of gonadotrophinindependent precocious puberty, as seen in McCune-Albright syndrome, and Leri-Weill dyschondrosteosis in a six and a half year-old girl. Her father also reports having early puberty and is similarly affected with dyschondrosteosis. This combination of features has not been reported previously, and represents the association of a skeletal dysplasia with an endocrinopathy.

Original language	English
Pages (from-to)	265-268
Number of pages	4
Journal	Journal of Pediatric Endocrinology and Metabolism
Volume	7
Issue number	3
DOIs	https://doi.org/10.1515/JPEM.1994.7.3.265
Publication status	Published - 1994

Keywords

dyschondrosteosis
McCune-Albright syndrome
precocious puberty
skeletal dysplasia

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10.1515/JPEM.1994.7.3.265

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abstract = "We present a case of gonadotrophinindependent precocious puberty, as seen in McCune-Albright syndrome, and Leri-Weill dyschondrosteosis in a six and a half year-old girl. Her father also reports having early puberty and is similarly affected with dyschondrosteosis. This combination of features has not been reported previously, and represents the association of a skeletal dysplasia with an endocrinopathy.",

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AU - Patel, Leena

AU - Clayton, Peter E.

AU - Super, Maurice

AU - Price, David A.

PY - 1994

Y1 - 1994

N2 - We present a case of gonadotrophinindependent precocious puberty, as seen in McCune-Albright syndrome, and Leri-Weill dyschondrosteosis in a six and a half year-old girl. Her father also reports having early puberty and is similarly affected with dyschondrosteosis. This combination of features has not been reported previously, and represents the association of a skeletal dysplasia with an endocrinopathy.

AB - We present a case of gonadotrophinindependent precocious puberty, as seen in McCune-Albright syndrome, and Leri-Weill dyschondrosteosis in a six and a half year-old girl. Her father also reports having early puberty and is similarly affected with dyschondrosteosis. This combination of features has not been reported previously, and represents the association of a skeletal dysplasia with an endocrinopathy.

KW - dyschondrosteosis

KW - McCune-Albright syndrome

KW - precocious puberty

KW - skeletal dysplasia

UR - https://www.scopus.com/pages/publications/0028108864

U2 - 10.1515/JPEM.1994.7.3.265

DO - 10.1515/JPEM.1994.7.3.265

M3 - Article

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AN - SCOPUS:0028108864

SN - 0334-018X

VL - 7

SP - 265

EP - 268

JO - Journal of Pediatric Endocrinology and Metabolism

JF - Journal of Pediatric Endocrinology and Metabolism

IS - 3

ER -

Gonadotrophin-independent precocious puberty and dyschondrosteosis

Abstract

Keywords

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