Browsing by Author "Cammarata-Scalisi, Francisco"

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Clinical and molecular study in a child with X-linked hypohidrotic ectodermal dysplasia

Callea, Michele; Yavuz, Izzet; Clarich, Gabriella; Cammarata-Scalisi, Francisco (Soc Argentina Pediatria, 2015)

Ectodermal dysplasia encompasses more than 200 clinically distinct entities, which affect at least two structures derived from the ectoderm, including the skin, hair, nails, teeth, sweat glands, and sebaceous glands. ...
Clinical and molecular study in a family with autosomal dominant hypohidrotic ectodermal dysplasia

Callea, Michele; Cammarata-Scalisi, Francisco; Willoughby, Colin E.; Giglio, Sabrina R.; Sani, Ilaria; Bargiacchi, Sara; Traficante, Giovanna (Soc Argentina Pediatria, 2017)

Hypohidrotic ectodermal dysplasia (HED) is a rare disease characterized by deficiency in development of structure derived from the ectoderm and is caused by mutations in the genes EDA, EDAR, or EDARADD. Phenotypes caused ...
Isotretinoin embryopathy. An entity that can be avoided

Cammarata-Scalisi, Francisco; Nieves, Dairelis; Avendano, Andrea; Lacruz-Rengel, Maria A.; Alviarez, Karelys; Davila, Francys; Yavuz, Izzet (Soc Argentina Pediatria, 2018)

Isotretinoin is the most effective drug in the treatment of severe recalcitrant nodulocystic acne. However, treatment with this drug is associated with adverse effects, the most severe being teratogenesis. It has been ...