Een zwelling van de onderkaak

J. de Lange; O. F. Norbruis

Een zwelling van de onderkaak

J. de Lange
, O. F. Norbruis

Research output: Contribution to journal › Article › Professional

Abstract

Nevoid basal cell carcinoma syndrome (NBCCS) is characterised by skeletal anomalies, cutaneous basal cell carcinomas and multiple keratocysts. NBCCS is an autosomal dominant disorder, but can have a variable phenotypic penetration. NBCCS can also arise spontaneously. The prevalence is 1:60.000 and 50-65% of patients with NBCCS have affected family members. A recently diagnosed patient is presented and the manifestations of the syndrome are discussed

Original language	Dutch
Pages (from-to)	298-301
Journal	Nederlands tijdschrift voor tandheelkunde
Volume	112
Issue number	8
Publication status	Published - 2005

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

SDG 3 Good Health and Well-being

Cite this

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title = "Een zwelling van de onderkaak",

abstract = "Nevoid basal cell carcinoma syndrome (NBCCS) is characterised by skeletal anomalies, cutaneous basal cell carcinomas and multiple keratocysts. NBCCS is an autosomal dominant disorder, but can have a variable phenotypic penetration. NBCCS can also arise spontaneously. The prevalence is 1:60.000 and 50-65\% of patients with NBCCS have affected family members. A recently diagnosed patient is presented and the manifestations of the syndrome are discussed",

author = "\{de Lange\}, J. and Norbruis, \{O. F.\}",

year = "2005",

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AU - de Lange, J.

AU - Norbruis, O. F.

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N2 - Nevoid basal cell carcinoma syndrome (NBCCS) is characterised by skeletal anomalies, cutaneous basal cell carcinomas and multiple keratocysts. NBCCS is an autosomal dominant disorder, but can have a variable phenotypic penetration. NBCCS can also arise spontaneously. The prevalence is 1:60.000 and 50-65% of patients with NBCCS have affected family members. A recently diagnosed patient is presented and the manifestations of the syndrome are discussed

AB - Nevoid basal cell carcinoma syndrome (NBCCS) is characterised by skeletal anomalies, cutaneous basal cell carcinomas and multiple keratocysts. NBCCS is an autosomal dominant disorder, but can have a variable phenotypic penetration. NBCCS can also arise spontaneously. The prevalence is 1:60.000 and 50-65% of patients with NBCCS have affected family members. A recently diagnosed patient is presented and the manifestations of the syndrome are discussed

M3 - Article

C2 - 16128217

SN - 0028-2200

VL - 112

SP - 298

EP - 301

JO - Nederlands tijdschrift voor tandheelkunde

JF - Nederlands tijdschrift voor tandheelkunde

IS - 8

ER -