Skin biopsy is helpful for the diagnosis of incontinentia pigmenti at late stage (IV): a series of 26 cutaneous biopsies
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Incontinentia pigmenti with defect in cellular immunity | Boletín Médico del Hospital Infantil de México (English Edition)
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SciELO - Brasil - Incontinentia pigmenti or Bloch-Sulzberger syndrome: a rare X-linked genodermatosis Incontinentia pigmenti or Bloch-Sulzberger syndrome: a rare X-linked genodermatosis
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SciELO - Brasil - Incontinentia pigmenti or Bloch-Sulzberger syndrome: a rare X-linked genodermatosis Incontinentia pigmenti or Bloch-Sulzberger syndrome: a rare X-linked genodermatosis
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Won W Shon on Twitter: "6 day old baby girl. Whorls of dyskeratotic keratinocytes + eosinophilic spongiosis = Incontinentia pigmenti #dermpath https://t.co/WdrqmPLFN4 https://t.co/V5XBzOosYk" / Twitter
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Phenotypic and genetic spectrum of incontinentia pigmenti – a large case series - Hübner - 2022 - JDDG: Journal der Deutschen Dermatologischen Gesellschaft - Wiley Online Library
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Incontinentia Pigmenti (Bloch-Siemens syndrome, Bloch-Sulzberger syndrome, Bloch-Sulzberger disease, melanoblastosis cutis, naevus pigmentosus systematicus) - Dermatology Advisor
Won W Shon on Twitter: "6 day old baby girl. Whorls of dyskeratotic keratinocytes + eosinophilic spongiosis = Incontinentia pigmenti #dermpath https://t.co/WdrqmPLFN4 https://t.co/V5XBzOosYk" / Twitter
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SciELO - Brasil - Incontinentia pigmenti or Bloch-Sulzberger syndrome: a rare X-linked genodermatosis Incontinentia pigmenti or Bloch-Sulzberger syndrome: a rare X-linked genodermatosis
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