ISSN:
1365-2214
Source:
Blackwell Publishing Journal Backfiles 1879-2005
Topics:
Medicine
,
Psychology
Notes:
Background Diagnosis of Nevoid Basal Cell Carcinoma Syndrome (NBCCS) in infants may pose significant challenges to clinicians owing to its variable expressivity and age-related manifestations.Methods We report two paediatric cases of NBCCS who presented initially with a non-specific phenotype.Results In case 1, a diagnosis of NBCCS was possible only after the father was interviewed and found to present with two major criteria for the disease. Subsequent molecular testing confirmed the diagnosis. In case 2, molecular testing of the infant and his father had diagnostic value as neither satisfied fully the current diagnostic criteria for NBCCS.Conclusions Presence of the few clinical manifestations of NBCCS that appear in infants, typically congenital malformations and skeletal abnormalities, should prompt clinicians to conduct in-person interviews with both parents. In general, paediatricians should refer both parents of infants who are suspected of having an inherited condition to clinical geneticists for expert examination, given the potential unreliability of reported medical history.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1111/j.1365-2214.2005.00514.x
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