Literature DB >> 20807362

Incontinentia pigmenti in a male infant with Klinefelter syndrome: a case report and review of the literature.

Evelina Buinauskaite1, Jurate Buinauskiene, Vesta Kucinskiene, Dale Strazdiene, Skaidra Valiukeviciene.   

Abstract

Incontinentia pigmenti, also known as Bloch-Sulzberger syndrome, is a hereditary, X-linked dominant disorder characterized by abnormalities of skin, hair, teeth, eyes, and the central nervous system. It is classically considered a male-lethal disorder leading to recurrent miscarriages of male fetuses. We report a rare case of a surviving baby boy with the classic clinical features of incontinentia pigmenti that can be explained by Klinefelter syndrome.
© 2010 Wiley Periodicals, Inc.

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Year:  2010        PMID: 20807362     DOI: 10.1111/j.1525-1470.2010.01261.x

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN: 0736-8046            Impact factor:   1.588


  10 in total

1.  Long-term follow-up of neurological manifestations in a boy with incontinentia pigmenti.

Authors:  Lucia Margari; Anna Linda Lamanna; Maura Buttiglione; Francesco Craig; Maria G Petruzzelli; Vanessa Terenzio
Journal:  Eur J Pediatr       Date:  2013-05-08       Impact factor: 3.183

2.  Absence of an osteopetrosis phenotype in IKBKG (NEMO) mutation-positive women: A case-control study.

Authors:  Morten Frost; Michaela Tencerova; Christina M Andreasen; Thomas L Andersen; Charlotte Ejersted; Dea Svaneby; Weimin Qui; Moustapha Kassem; Allahdad Zarei; William H McAlister; Deborah J Veis; Michael P Whyte; Anja L Frederiksen
Journal:  Bone       Date:  2019-01-16       Impact factor: 4.398

3.  X-Linked agammaglobulinemia in a child with Klinefelter's syndrome.

Authors:  Alexis-Virgil Cochino; Ales Janda; Barbora Ravcukova; Vasilica Plaiasu; Diana Ochiana; Ioan Gherghina; Tomas Freiberger
Journal:  J Clin Immunol       Date:  2014-01-30       Impact factor: 8.317

4.  A healthy delivery of twins by assisted reproduction followed by preimplantation genetic screening in a woman with X-linked dominant incontinentia pigmenti.

Authors:  Myung Joo Kim; Sang Woo Lyu; Hyun Ha Seok; Ji Eun Park; Sung Han Shim; Tae Ki Yoon
Journal:  Clin Exp Reprod Med       Date:  2014-12-31

5.  Incontinentia Pigmenti: A Case Report of a Complex Systemic Disease.

Authors:  Serena Gianfaldoni; Georgi Tchernev; Uwe Wollina; Torello Lotti
Journal:  Open Access Maced J Med Sci       Date:  2017-07-23

6.  Pulmonary hypertension and vasculopathy in incontinentia pigmenti: a case report.

Authors:  Abduljabbar Alshenqiti; Marwan Nashabat; Hissah AlGhoraibi; Omar Tamimi; Majid Alfadhel
Journal:  Ther Clin Risk Manag       Date:  2017-05-09       Impact factor: 2.423

Review 7.  Human Genetic Diseases Linked to the Absence of NEMO: An Obligatory Somatic Mosaic Disorder in Male.

Authors:  Alessandra Pescatore; Ezia Spinosa; Carmela Casale; Maria Brigida Lioi; Matilde Valeria Ursini; Francesca Fusco
Journal:  Int J Mol Sci       Date:  2022-01-21       Impact factor: 5.923

8.  Androgenetic Alopecia in a Patient with Klinefelter Syndrome: Case Report and Literature Review.

Authors:  Waleed Alsalhi; Antonella Tosti
Journal:  Skin Appendage Disord       Date:  2020-12-07

Review 9.  Systemic and ocular manifestations of a patient with mosaic ARID1A-associated Coffin-Siris syndrome and review of select mosaic conditions with ophthalmic manifestations.

Authors:  Virginia Miraldi Utz; Diana S Brightman; Monica A Sandoval; Robert B Hufnagel; Howard M Saal
Journal:  Am J Med Genet C Semin Med Genet       Date:  2020-09-05       Impact factor: 3.359

10.  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
  10 in total

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