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Epidermal Nevous in Association with Some Uncommon Manifestations

Nima Rezaei

Puni tekst: engleski, PDF (139 KB) str. 0-0 preuzimanja: 314* citiraj
APA 6th Edition
Rezaei, N. (2013). Epidermal Nevous in Association with Some Uncommon Manifestations. Acta Dermatovenerologica Croatica, 21 (4), 0-0. Preuzeto s https://hrcak.srce.hr/116003
MLA 8th Edition
Rezaei, Nima. "Epidermal Nevous in Association with Some Uncommon Manifestations." Acta Dermatovenerologica Croatica, vol. 21, br. 4, 2013, str. 0-0. https://hrcak.srce.hr/116003. Citirano 17.10.2021.
Chicago 17th Edition
Rezaei, Nima. "Epidermal Nevous in Association with Some Uncommon Manifestations." Acta Dermatovenerologica Croatica 21, br. 4 (2013): 0-0. https://hrcak.srce.hr/116003
Harvard
Rezaei, N. (2013). 'Epidermal Nevous in Association with Some Uncommon Manifestations', Acta Dermatovenerologica Croatica, 21(4), str. 0-0. Preuzeto s: https://hrcak.srce.hr/116003 (Datum pristupa: 17.10.2021.)
Vancouver
Rezaei N. Epidermal Nevous in Association with Some Uncommon Manifestations. Acta Dermatovenerol Croat. [Internet]. 2013 [pristupljeno 17.10.2021.];21(4):0-0. Dostupno na: https://hrcak.srce.hr/116003
IEEE
N. Rezaei, "Epidermal Nevous in Association with Some Uncommon Manifestations", Acta Dermatovenerologica Croatica, vol.21, br. 4, str. 0-0, 2013. [Online]. Dostupno na: https://hrcak.srce.hr/116003. [Citirano: 17.10.2021.]

Sažetak

Epidermal nevus syndrome (ENS) is a rare disorder, characterized with congenital epidermal nevi in association with several abnormalities in different organs.

Herein, an infant with EN is presented who suffered from various manifestations, including aplasia cutis congenital, congenital hemangioma, ambiguous genitalia, mislocated anus, and growth retardation. Skin biopsy showed dysmorphic folliculosebaceous apparatus in the dermis and hypertrichosis, compatible with organoid nevus. No mutations were found in FGFR3, PIK3CA, NRAS, HRAS and KRAS genes.

Although the diagnosis of ENS is made for the patient, association of some rare manifestations could suggest either presence of mutation in an unknown gene or an undefined syndrome with manifestations resembling ENS.

Hrčak ID: 116003

URI
https://hrcak.srce.hr/116003

Posjeta: 503 *