Hand-foot-genital syndrome - analysis of two cases
- PMID: 29638102
- PMCID: PMC5982563
- DOI: 10.5935/1518-0557.20180025
Hand-foot-genital syndrome - analysis of two cases
Abstract
Hand-food-genital syndrome (HFGS) is a rare genetic condition. This report describes the cases of two patients, aged 33 and 15, presenting related somatic abnormalities. HFGS stems from an autosomal anomaly linked to the HOXA 13 gene. Therapeutic procedures are discussed in order to identify the best treatment approach to the patients, as well as possible conditioning genetic anomalies.
Keywords: Autosomal abnormalities; Hand-food-genital syndrome.; Urogenital abnormalities.
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