Aplasia cutis congénita tipo I: aporte de un caso / Aplasia cutis congenita: a case report
Rev. chil. dermatol
;
27(2): 212-217, 2011. ilus
Article
in Spanish
| LILACS
| ID: lil-645032
RESUMEN
La Aplasia Cutis Congénita, es un grupo heterogéneo de alteraciones que consisten en la falta congénita localizada o extensa, de piel, que puede acompañarse de ausencia de estructuras subyacentes. Su apariencia clínica es variable y su origen es multifactorial. Presentamos el caso de un recién nacido con Aplasia Cutis Congénita, sin antecedentes familiares de esta enfermedad ni historia de uso materno de drogas, en quien no se constataron hallazgos extracutáneos.
ABSTRACT
Congenital aplasia cutis, is a heterogeneous group of disorders that involve the congenital absence, localized or extensive, of the skin, which may be accompanied by the absence of underlying structures. Its clinical appareance is variable with a multifactorial origin. We report the case of a newborn with Congenital Aplasia Cutis with no family history of the disease or history of maternal drug abuse, in whom extracutaneous findings were not found.
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Index:
LILACS (Americas)
Main subject:
Ectodermal Dysplasia
Type of study:
Diagnostic study
Limits:
Humans
/
Male
/
Infant, Newborn
Language:
Spanish
Journal:
Rev. chil. dermatol
Journal subject:
Dermatology
Year:
2011
Type:
Article
Affiliation country:
Paraguay
Institution/Affiliation country:
Universidad Nacional de Asunción/CL
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