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DOCK8 Mutation Syndrome: A Diagnostic Challenge for Dermatologists.

Acta dermato-venereologica - 2 Nov 2016

Moreau Joséphine, Beaussant-Cohen Sarah, Aubin François, Rohrlich Pierre-Simon, Puzenat Eve

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Identifiers

PMID: 26573532
DOI: 10.2340/00015555-2288

Genes

DOCK8

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A novel homozygous DOCK8 mutation associated with unusual coexistence of gross molluscum contagiosum and epidermodysplasia verruciformis in a DOCK8 deficiency patient.Semantic proximity Read ↗

Clinical and molecular profile of 20 patients with DOCK8 deficiency-a single-center experience from Southern India.Semantic proximity Read ↗

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SPINK5: both rare and common skin disease.Semantic proximity Read ↗

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Cutaneous manifestations of DOCK8 deficiency syndrome.Semantic proximity Read ↗

Clinically focused exome sequencing identifies an homozygous mutation that confers DOCK8 deficiency.Semantic proximity Read ↗

Cutaneous clues: a genetic disorder diagnosed by dermatologic findings.Semantic proximity Read ↗

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