Porokeratotic eccrine ostial and dermal duct nevus associated with an 11 megabase 3p deletion.

Castle, Alison M R; Ramien, Michele L; Kanigsberg, Nordau; El Demellawy, Dina; McGowan-Jordan, Jean; Beaulieu Bergeron, Melanie; Armour, Christine M

Castle, Alison M R; Ramien, Michele L; Kanigsberg, Nordau; El Demellawy, Dina; McGowan-Jordan, Jean; Beaulieu Bergeron, Melanie; Armour, Christine M.

Afiliación

Castle AMR; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
Ramien ML; Division of Community Pediatrics, Department of Pediatrics, Alberta Children's Hospital, Calgary, Alberta, Canada.
Kanigsberg N; Division of Dermatology and Rheumatology, Department of Pediatrics, University of Ottawa, Ottawa, Ontario, Canada.
El Demellawy D; Department of Pathology and Laboratory Medicine, University of Ottawa, Ottawa, Ontario, Canada.
McGowan-Jordan J; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.
Beaulieu Bergeron M; Department of Pathology and Laboratory Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Armour CM; Department of Genetics, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.

Pediatr Dermatol ; 39(1): 107-111, 2022 Jan.

Article en En | MEDLINE | ID: mdl-34929758

Asunto(s)

Hamartoma; Nevo; Poroqueratosis; Neoplasias Cutáneas; Enfermedades de las Glándulas Sudoríparas; Glándulas Ecrinas; Humanos; Poroqueratosis/genética

Palabras clave

3p26.3p25.3 deletion; PEODDN; cytogenetics; genetic diseases/mechanisms; mosaicism

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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Enfermedades de las Glándulas Sudoríparas / Poroqueratosis / Hamartoma / Nevo Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Pediatr Dermatol Año: 2022 Tipo del documento: Article País de afiliación: Canadá

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