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Acta Dermatovenerologica Croatica, Vol. 21 No. 3, 2013.

Ostalo

Incontinentia Pigmenti: Case Report

Xiuli Li ; PhD of The Second Military Medical University, committee member of Shanghai Institute of Microbiology, Attending doctor
Xiuxiu Wang ; Bachelor degree of Clinic Medicine, Tongji University
Yulin Shi

Puni tekst: engleski PDF 240 Kb

str. 193-193

preuzimanja: 1.405

citiraj

Sažetak

Incontinentia pigmenti (IP) or Bloch-Sulzberger syndrome, is a rare X linked dominant disorder with characteristic skin, hair, eye, dental and neurological abnormalities mostly affecting females. We reported two cases of newborn female children exhibiting characteristic cutaneous and neurological findings with one year follow-up.

Ključne riječi

incontinentia pigmenti; NEMO/IKBKG; newborn

Hrčak ID:

109928

URI

https://hrcak.srce.hr/109928

Datum izdavanja:

29.10.2013.

Posjeta: 1.920 *