Premium
Childhood alopecia areata—Data from the National Alopecia Areata Registry
Author(s) -
WohlmuthWieser Iris,
Osei Joyce S.,
Norris David,
Price Vera,
Hordinsky Maria K.,
Christiano Angela,
Duvic Madeleine
Publication year - 2018
Publication title -
pediatric dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.542
H-Index - 73
eISSN - 1525-1470
pISSN - 0736-8046
DOI - 10.1111/pde.13387
Subject(s) - alopecia areata , medicine , dermatology , family history , hair loss , atopic dermatitis , pediatrics , surgery
Background/Objectives Alopecia areata may occur at any age and is the third‐most‐common dermatosis in children. The objective of this study was to investigate the clinical and epidemiologic features of children and adolescents with alopecia areata based on the data of the National Alopecia Areata registry on children and adolescents. Methods Two thousand two hundred eighteen children and adolescents with alopecia areata self‐enrolled in the National Alopecia Areata Registry and completed a web‐based, self‐administered, short‐intake screening questionnaire (first tier). In the second tier, 643 patients participated in a clinical examination and completed a long‐form questionnaire. Results Mean age of onset was 5.9 ± 4.1 years. With a female to male ratio of 1.5:1, alopecia areata was more prevalent in girls, but boys were significantly more likely to have a severe type ( P = .009). One‐fourth of all children had a positive family history, with 8% having more than three affected relatives. The disease most commonly associated with alopecia areata was atopic dermatitis (32.7%). Conclusion Childhood alopecia areata is more prevalent in girls than in boys, but boys have more extensive alopecia areata. Despite the low prevalence, congenital alopecia areata is an important differential diagnosis for neonatal hair loss. Alopecia areata runs in families, suggesting an underlying genetic background. One‐quarter of the children reported at least one affected first‐degree relative; 8% had more than three affected relatives.