Literature DB >> 27493406

The neurologic aspects of hypomelanosis of Ito: Case report and review of the literature.

Amal Y Kentab1, Hamdy H Hassan2, Muddathir H A Hamad1, Ahmed Alhumidi3.   

Abstract

The term hypomelanosis of Ito (HI) is applied to individuals with skin hypopigmentation along the lines of Blaschko. Although it was originally described as a purely cutaneous disease, subsequent studies describing HI reported a 33% to 94% association with multiple extracutaneous manifestations, mostly of the central nervous and musculoskeletal systems. This leads to characterization of HI as a neurocutaneous disorder. We report a 10-year-old boy who presented with constellation of multiple congenital anomalies including facial dysmorphism, skin hypopigmentation, musculoskeletal, and nervous system abnormalities. The latter manifested as hypotonia, generalized seizures, and mild mental retardation. Cranial magnetic resonance imaging revealed normal finding initially, however; follow-up diffusion weighted images were suggestive of a possible iron accumulation. The facial phenotype coupled with the bilateral globus pallidi lesions were never been reported in association with HI. Thus, our patient represents a possible novel example of HI.

Entities:  

Keywords:  Brain iron accumulation; Hypomelanosis of Ito; Neurocutaneous syndrome

Year:  2014        PMID: 27493406      PMCID: PMC4949800     

Source DB:  PubMed          Journal:  Sudan J Paediatr        ISSN: 0256-4408


  42 in total

1.  Karak syndrome: a novel degenerative disorder of the basal ganglia and cerebellum.

Authors:  A Mubaidin; E Roberts; D Hampshire; M Dehyyat; A Shurbaji; M Mubaidien; A Jamil; A Al-Din; A Kurdi; C G Woods
Journal:  J Med Genet       Date:  2003-07       Impact factor: 6.318

2.  Insights into the pathogenesis of cerebral lesions in incontinentia pigmenti.

Authors:  Sabine J Hennel; Paul G Ekert; Joseph J Volpe; Terrie E Inder
Journal:  Pediatr Neurol       Date:  2003-08       Impact factor: 3.372

Review 3.  Abnormal pigmentation in hypomelanosis of Ito and pigmentary mosaicism: the role of pigmentary genes.

Authors:  S M Taibjee; D C Bennett; C Moss
Journal:  Br J Dermatol       Date:  2004-08       Impact factor: 9.302

4.  Neurosurgical management of medically intractable epilepsy associated with hypomelanosis of Ito.

Authors:  Dimitris G Placantonakis; Gershon Ney; Mark Edgar; Mark Souweidane; Syed Hosain; Theodore H Schwartz
Journal:  Epilepsia       Date:  2005-02       Impact factor: 5.864

Review 5.  Hypomelanosis of Ito and X;autosome translocations: a unifying hypothesis.

Authors:  E Hatchwell
Journal:  J Med Genet       Date:  1996-03       Impact factor: 6.318

6.  Regional cortical dysplasia associated with suspected hypomelanosis of Ito.

Authors:  J Ono; K Harada; R Kodaka; M Ishida; S Okada
Journal:  Pediatr Neurol       Date:  1997-10       Impact factor: 3.372

7.  Hypomelanosis of ITO. A study of 76 infantile cases.

Authors:  I Pascual-Castroviejo; C Roche; A Martinez-Bermejo; J Arcas; V Lopez-Martin; A Tendero; J L Esquiroz; S I Pascual-Pascual
Journal:  Brain Dev       Date:  1998-01       Impact factor: 1.961

Review 8.  Heterogeneous seizure manifestations in Hypomelanosis of Ito: report of four new cases and review of the literature.

Authors:  Komi Assogba; Edoardo Ferlazzo; Pasquale Striano; Tiziana Calarese; Nathalie Villeneuve; Ivan Ivanov; Placido Bramanti; Edoardo Sessa; Iliana Pacheva; Pierre Genton
Journal:  Neurol Sci       Date:  2009-11-10       Impact factor: 3.307

9.  Hypomelanosis of Ito and Sturge-Weber syndrome without facial nevus: an association or a new syndrome?

Authors:  Aydan Değerliyurt; Asli Kantar; Serdar Ceylaner; Sabiha Aysun
Journal:  Pediatr Neurol       Date:  2009-05       Impact factor: 3.372

10.  Autism and hypomelanosis of Ito in twins.

Authors:  M Zappella
Journal:  Dev Med Child Neurol       Date:  1993-09       Impact factor: 5.449

View more
  3 in total

1.  Hypomelanosis of Ito: streaks and whorls.

Authors:  Daisy Khera; Saurabh Singh; Priya Gupta
Journal:  BMJ Case Rep       Date:  2019-04-23

2.  Hypomelanosis of Ito with gynaecomastia and dental anomaly.

Authors:  Mudita Gupta; Pragya Gupta; Reena Sharma; Archit Gupta
Journal:  BMJ Case Rep       Date:  2018-07-06

3.  Genetic and clinical characterization of 73 Pigmentary Mosaicism patients: revealing the genetic basis of clinical manifestations.

Authors:  C Salas-Labadía; S Gómez-Carmona; R Cruz-Alcívar; D Martínez-Anaya; V Del Castillo-Ruiz; C Durán-McKinster; V Ulloa-Avilés; E Yokoyama-Rebollar; A Ruiz-Herrera; P Navarrete-Meneses; E Lieberman-Hernández; A González-Del Angel; D Cervantes-Barragán; C Villarroel-Cortés; A Reyes-León; D Suárez-Pérez; A Pedraza-Meléndez; A González-Orsuna; P Pérez-Vera
Journal:  Orphanet J Rare Dis       Date:  2019-11-15       Impact factor: 4.123

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.