SHORT syndrome in a two-year-old girl – case report

BACKGROUND: SHORT syndrome is a rare genetic congenital defects condition. The frequency of the disease still remains unknown. CASE PRESENTATION: We report the two-year-four-month old female with SHORT syndrome who present growth retardation and dysmorphic features (triangular-shaped face, prominent...

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Detalles Bibliográficos
Autores principales: Klatka, Maria, Rysz, Izabela, Kozyra, Katarzyna, Polak, Agnieszka, Kołłątaj, Witold
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5418728/
https://www.ncbi.nlm.nih.gov/pubmed/28472977
http://dx.doi.org/10.1186/s13052-017-0362-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5418728/
https://www.ncbi.nlm.nih.gov/pubmed/28472977
http://dx.doi.org/10.1186/s13052-017-0362-z

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