Recombinant growth hormone therapy in a girl with costello syndrome: a 4-year observation

BACKGROUND: Costello syndrome is a rare syndrome of multiple congenital anomalies. The typical clinical traits include dysmorphic craniofacial features, skin hyperpigmentation and excess, feeding difficulties leading to severe postnatal growth retardation, short stature, joint hypermobility, and del...

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Detalles Bibliográficos
Autores principales: Blachowska, Ewa, Petriczko, Elżbieta, Horodnicka-Józwa, Anita, Skórka, Agata, Pelc, Magdalena, Krajewska-Walasek, Małgorzata, Walczak, Mieczysław
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4729164/
https://www.ncbi.nlm.nih.gov/pubmed/26812928
http://dx.doi.org/10.1186/s13052-015-0209-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4729164/
https://www.ncbi.nlm.nih.gov/pubmed/26812928
http://dx.doi.org/10.1186/s13052-015-0209-4

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