Literature DB >> 10832484

Hypomelanosis of Ito.

A Kumar1, D Chaudhary, V Bhargava.   

Abstract

A two-year-old male child presented with bizarre hypopigmented skin lesions, severe mental retardation and generalized tonic-clonic seizures. Examination showed hypopigmented patterned whorls and irregular patches over the trunk and linear streaks over the flexor aspects of upper and lower limbs. He also had generalized hypertonia and brisk tendon reflexes. Other systems were normal.

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Year:  1996        PMID: 10832484     DOI: 10.1007/bf02905740

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


  6 in total

Review 1.  Unusual neurocutaneous syndromes.

Authors:  B O Berg
Journal:  Neurol Clin       Date:  1985-02       Impact factor: 3.806

2.  Diploid/triploid mixoploidy and hypomelanosis of Ito.

Authors:  D Donnai; C McKeown; T Andrews; A P Read
Journal:  Lancet       Date:  1986-06-21       Impact factor: 79.321

3.  Incontinentia pigmenti et achromians.

Authors:  R Mittal; F Handa; S C Sharma
Journal:  Dermatologica       Date:  1975

4.  Hypomelanosis of Ito (incontinentia pigmenti achromians): a neurocutaneous syndrome.

Authors:  M F Schwartz; N B Esterly; D F Fretzin; E Pergament; I H Rozenfeld
Journal:  J Pediatr       Date:  1977-02       Impact factor: 4.406

5.  Incontinentia pigmenti achromians (Ito).

Authors:  H Takematsu; S Sato; M Igarashi; M Seiji
Journal:  Arch Dermatol       Date:  1983-05

6.  Hypomelanosis of Ito associated with chromosomal translocation involving Xp11.

Authors:  M S Lungarotti; C Martello; A Calabro; F Baldari; G Mariotti
Journal:  Am J Med Genet       Date:  1991-09-15
  6 in total

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