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Incontinentia pigmenti en Cajamarca: reporte de un caso en lactante / Incontinentia pigmenti in Cajamarca: a case report on infant
Galvez-Marticorena, Brayan; Chambi-Torres, Javier.
  • Galvez-Marticorena, Brayan; Universidad de San Martín de Porres. Lima. PE
  • Chambi-Torres, Javier; Universidad de San Martín de Porres. Lima. PE
Horiz. méd. (Impresa) ; 15(3): 57-60, jul.-set. 2015. ilus
Article in Spanish | LILACS, LIPECS | ID: lil-781150
RESUMEN
La Incontinentia pigmenti (IP) o Síndrome de Bloch-Sulzberger es una rara enfermedad dominante ligada al cromosoma X, caracterizada por lesiones en la piel. Puede estar acompañada de manifestaciones neurológicas, oftalmológicas y dentales. Se presenta el caso clínico de una lactante de un mes y veintiséis días diagnosticada con esta enfermedad y tratada con éxito...
ABSTRACT
Incontinentia pigmenti (IP) or Bloch-SuIzberger syndrome is a rare dominant X-linked disease characterized by skin lesions. lt may be accompanied by neurological, ophthalmological and dental manifestations. We report the case of a one month and twenty Six days old female patient diagnosed with this disease who was successfully treated...
Subject(s)
Full text: Available Index: LILACS (Americas) Main subject: Skin Abnormalities / Incontinentia Pigmenti / Hyperpigmentation Limits: Female / Humans / Infant, Newborn Language: Spanish Journal: Horiz. méd. (Impresa) Year: 2015 Type: Article Institution/Affiliation country: Universidad de San Martín de Porres/PE

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Full text: Available Index: LILACS (Americas) Main subject: Skin Abnormalities / Incontinentia Pigmenti / Hyperpigmentation Limits: Female / Humans / Infant, Newborn Language: Spanish Journal: Horiz. méd. (Impresa) Year: 2015 Type: Article Institution/Affiliation country: Universidad de San Martín de Porres/PE