Literature DB >> 24183225

Incontinentia pigmenti: case report.

Xiuli Li1, Xiuxiu Wang, Junying Gu, Zhiyu Liu, Yuling Shi.   

Abstract

Incontinentia pigmenti or Bloch-Sulzberger syndrome is a rare X-linked dominant disorder with characteristic skin, hair, eye, dental and neurologic abnormalities mostly affecting females. We report a case of a female newborn exhibiting characteristic cutaneous and neurologic findings with one-year follow-up.

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Year:  2013        PMID: 24183225

Source DB:  PubMed          Journal:  Acta Dermatovenerol Croat        ISSN: 1330-027X            Impact factor:   1.256


  3 in total

1.  Incontinentia Pigmenti; a Rare Multisystem Disorder: Case Report of a 10-Year-Old Girl.

Authors:  Rezvan Rafatjoo; Amene Taghdisi Kashani
Journal:  J Dent (Shiraz)       Date:  2016-09

2.  A 6-Month-Old Girl with Incontinentia Pigmenti Presenting as Status Epilepticus.

Authors:  Moon Young Seo; Su Jeong You; Soung Hee Kim; Woo Ho Cho; Jong Hee Chae
Journal:  J Epilepsy Res       Date:  2017-12-31

3.  Incontinentia Pigmenti Misdiagnosed as Neonatal Herpes Simplex Virus Infection.

Authors:  Fahimeh Abdollahimajd; Minoo Fallahi; Mohammad Kazemian; Yalda Nilipour; Mitra Radfar; Sedigheh Tahereh Tehranchi
Journal:  Case Rep Pediatr       Date:  2018-06-13
  3 in total

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