Incontinentia Pigmenti (cont.)Medical Author:
Andrew A. Dahl, MD, FACS
Andrew A. Dahl, MD, FACSAndrew A. Dahl, MD, is a board-certified ophthalmologist. Dr. Dahl's educational background includes a BA with Honors and Distinction from Wesleyan University, Middletown, CT, and an MD from Cornell University, where he was selected for Alpha Omega Alpha, the national medical honor society. He had an internal medical internship at the New York Hospital/Cornell Medical Center. Medical Editor:
Melissa Conrad Stöppler, MD, Chief Medical Editor
Melissa Conrad Stöppler, MD, Chief Medical EditorMelissa Conrad Stöppler, MD, is a U.S. board-certified Anatomic Pathologist with subspecialty training in the fields of Experimental and Molecular Pathology. Dr. Stöppler's educational background includes a BA with Highest Distinction from the University of Virginia and an MD from the University of North Carolina. She completed residency training in Anatomic Pathology at Georgetown University followed by subspecialty fellowship training in molecular diagnostics and experimental pathology. IN THIS ARTICLEMultimediaMedia file 1: A 20-day-old female neonate with incontinentia pigmenti. Bullae and vesicles, as well as verrucous lesions, are seen on the lower extremities and buttock.
Media type: Photo Media file 2: A 27-day-old female neonate who first presented with incontinentia pigmenti when she was aged 20 days. Note the verrucous eruptions with brownish pigmentation in a streaky linear pattern on the left leg.
Media type: Photo Media file 3: Linear streak of pigmentation and erythematous vesicles on the left arm.
Media type: Photo Media file 4: Streaks of hyperpigmentation on the chest and right arm.
Media type: Photo |
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Incontinentia Pigmenti »
Incontinentia pigmenti (IP) is an X-linked dominant neurocutaneous syndrome with cutaneous, neurologic, ophthalmologic, and dental manifestations.
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