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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...
Autores principales: | Klatka, Maria, Rysz, Izabela, Kozyra, Katarzyna, Polak, Agnieszka, Kołłątaj, Witold |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
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 |
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