Xp microdeletion syndrome characterized by pathognomonic linear skin defects on the head and neck
B R Paulger1, E W Kraus, D R Pulitzer
1Division of Dermatology, University of Texas Health Science Center, San Antonio 78284, USA.
Pediatric Dermatology
|January 1, 1997
Abstract:
We describe a new case of a rare syndrome characterized by ocular abnormalities and pathognomonic linear skin defects. This syndrome is the result of an unbalanced translocation resulting in a deletion of the distal end of the short arm of the X chromosome. We report the thirteenth case and review the clinical and cytogenetic aspects of this disorder. In addition we discuss new findings pertaining to the histopathology of the skin lesions.
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