SAT-303 Combined Treatment of Gonadotropin Releasing Hormone Agonist and Recombinant Human Growth Hormone in Cental Precocious Puberty Patient with Underlying Leri Weill Dyschondrosteosis

Leri-Weill dyschondrosteosis (LWD) is a rare genetic disorder of bony growth characterized by abnormal shortening of the forearms and lower legs, abnormal misalignment of the wrist (Madelung deformity), and associated short stature. As a result of shortened leg bones, LMD patients typically have sho...

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Detalles Bibliográficos
Autores principales: Choi, Ju-hee, Kim, Dae Hyun, Suh, Chae-ri, Kim, So Yeon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2019
Materias:
Pediatric Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551925/
http://dx.doi.org/10.1210/js.2019-SAT-303

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551925/
http://dx.doi.org/10.1210/js.2019-SAT-303

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