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

Other

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

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page 193-193

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Abstract

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.

Keywords

incontinentia pigmenti; NEMO/IKBKG; newborn

Hrčak ID:

109928

URI

https://hrcak.srce.hr/109928

Publication date:

29.10.2013.

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