PMID- 19841399 OWN - NLM STAT- MEDLINE DCOM- 20091110 LR - 20191210 IS - 1538-3652 (Electronic) IS - 0003-987X (Linking) VI - 145 IP - 10 DP - 2009 Oct TI - Practical guidelines for evaluation of loose anagen hair syndrome. PG - 1123-8 LID - 10.1001/archdermatol.2009.220 [doi] AB - OBJECTIVES: To better categorize the epidemiologic profile, clinical features, and disease associations of loose anagen hair syndrome (LAHS) compared with other forms of childhood alopecia. DESIGN: Retrospective survey. SETTING: Academic pediatric dermatology practice. Patients Three hundred seventy-four patients with alopecia referred from July 1, 1997, to June 31, 2007. MAIN OUTCOME MEASURES: Epidemiologic data for all forms of alopecia were ascertained, such as sex, age at onset, age at the time of evaluation, and clinical diagnosis. Patients with LAHS were further studied by the recording of family history, disease associations, hair-pull test or biopsy results, hair color, laboratory test result abnormalities, initial treatment, and involvement of eyelashes, eyebrows, and nails. RESULTS: Approximately 10% of all children with alopecia had LAHS. The mean age (95% confidence interval) at onset differed between patients with LAHS (2.8 [1.2-4.3] years) vs patients without LAHS (7.1 [6.6-7.7] years) (P < .001), with 3 years being the most common age at onset for patients with LAHS. All but 1 of 37 patients with LAHS were female. The most common symptom reported was thin, sparse hair. Family histories were significant for LAHS (n = 1) and for alopecia areata (n = 3). In 32 of 33 patients, trichograms showed typical loose anagen hairs. Two children had underlying genetic syndromes. No associated laboratory test result abnormalities were noted among patients who underwent testing. CONCLUSIONS: Loose anagen hair syndrome is a common nonscarring alopecia in young girls with a history of sparse or fine hair. Before ordering extensive blood testing in young girls with diffusely thin hair, it is important to perform a hair-pull test, as a trichogram can be instrumental in the confirmation of a diagnosis of LAHS. FAU - Cantatore-Francis, Julie L AU - Cantatore-Francis JL AD - Department of Dermatology, New York University School of Medicine, New York University Medical Center, New York, NY 10016, USA. FAU - Orlow, Seth J AU - Orlow SJ LA - eng PT - Comparative Study PT - Evaluation Study PT - Journal Article PL - United States TA - Arch Dermatol JT - Archives of dermatology JID - 0372433 SB - IM MH - Age of Onset MH - Alopecia/*diagnosis/*epidemiology/genetics MH - Child MH - Child, Preschool MH - Cohort Studies MH - Confidence Intervals MH - Female MH - Follow-Up Studies MH - *Guidelines as Topic MH - Hair/abnormalities/*ultrastructure MH - Humans MH - Incidence MH - Infant MH - Microscopy, Electron MH - Probability MH - Retrospective Studies MH - Risk Factors MH - Severity of Illness Index MH - Syndrome EDAT- 2009/10/21 06:00 MHDA- 2009/11/11 06:00 CRDT- 2009/10/21 06:00 PHST- 2009/10/21 06:00 [entrez] PHST- 2009/10/21 06:00 [pubmed] PHST- 2009/11/11 06:00 [medline] AID - 145/10/1123 [pii] AID - 10.1001/archdermatol.2009.220 [doi] PST - ppublish SO - Arch Dermatol. 2009 Oct;145(10):1123-8. doi: 10.1001/archdermatol.2009.220.