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Infantile spasms and pigmentary mosaicism
Author(s) -
Hansen Lars K.,
Bygum Anette,
Krogh Lotte N.
Publication year - 2010
Publication title -
epilepsia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.687
H-Index - 191
eISSN - 1528-1167
pISSN - 0013-9580
DOI - 10.1111/j.1528-1167.2009.02475.x
Subject(s) - etiology , medicine , epileptic spasms , karyotype , dermatology , pediatrics , pathology , chromosome , epilepsy , biology , psychiatry , genetics , gene
Summary We present a 3‐year‐old boy with pigmentary mosaicism and persistent intractable infantile spasms due to mosaicism of chromosome 7. Getting the diagnosis of pigmentary mosaicism in a child with infantile spasms may not be easy, as most diagnostic work‐up is done in infancy, at a time when skin manifestations can be subtle. We stress the need for a meticulous search for an etiology in cases of infantile spasms. Diagnostic work‐up should include a dermatologic evaluation with skin biopsies for fibroblast culture (and karyotyping) from abnormal pigmented skin areas.

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