1.
Rev. cienc. med. Pinar Rio
;
22(4): 154-170, jul..-ago. 2018. ilus
Artigo
em Espanhol
| LILACS
| ID: biblio-959643
2.
Rev. cienc. med. Pinar Rio
;
16(2): 247-254, mar.-abr. 2012.
Artigo
em Espanhol
| LILACS
| ID: lil-739791
RESUMO
Se presenta un niño con trastorno de la pigmentación de la piel. Posee antecedentes familiares de igual entidad. A través de la confección de la historia clínica, confección del árbol genealógico, y fundamentalmente, el examen físico se le diagnóstica de piebaldismo. Se trata de una rara entidad, por lo tanto, se decide la revisión de la literatura médica.
A child presenting a pigmentary disorder in the skin attended to the genetic office, the patient has a familial history with the same entity. Through the preparation of the clinical chart, family tree was examined; Piebaldism was mainly diagnosed by physical examination. Since this is a rare entity, a medical literature revision was carried out.