Atypical dermal melanocytosis: a diagnostic clue in constitutional mismatch repair deficiency syndrome.

Polubothu, S; Scott, R H; Vabres, P; Kinsler, V A

Polubothu, S; Scott, R H; Vabres, P; Kinsler, V A.

Affiliation

Polubothu S; Paediatric Dermatology Department, Great Ormond Street Hospital for Children, London, U.K.
Scott RH; Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, UCL, London, U.K.
Vabres P; Clinical Genetics Department, Great Ormond Street Hospital for Children, London, U.K.
Kinsler VA; Equipe d'Accueil 4271, Génétique des Anomalies du Développement, Université de Bourgogne Franche-Comté, Dijon, France.

Br J Dermatol ; 177(5): e185-e186, 2017 11.

Article in En | MEDLINE | ID: mdl-28369758

Subject(s)

Brain Neoplasms/diagnosis; Colorectal Neoplasms/diagnosis; DNA-Binding Proteins/genetics; Melanosis/etiology; Neoplastic Syndromes, Hereditary/diagnosis; Brain Neoplasms/genetics; Colorectal Neoplasms/genetics; Consanguinity; Female; Humans; Infant; Melanosis/genetics; Neoplastic Syndromes, Hereditary/genetics; Neurocutaneous Syndromes/diagnosis; Neurocutaneous Syndromes/genetics

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Neoplastic Syndromes, Hereditary / Brain Neoplasms / Colorectal Neoplasms / DNA-Binding Proteins / Melanosis Type of study: Diagnostic_studies Limits: Female / Humans / Infant Language: En Journal: Br J Dermatol Year: 2017 Document type: Article

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