Literature DB >> 11939812

Is the loose anagen hair syndrome a keratin disorder? A clinical and molecular study.

Valérie Chapalain1, Hermelita Winter, Lutz Langbein, Jean-Michel Le Roy, Christine Labrèze, Milos Nikolic, Jürgen Schweizer, Alain Taïeb.   

Abstract

OBJECTIVES: To report the clinical features of the loose anagen hair syndrome and to test the hypothesis that the typical gap between the hair and the inner root sheath may result from hereditary defects in the inner root sheath or the apposed companion layer.
DESIGN: Case series.
SETTING: A pediatric dermatology unit (referral center). PATIENTS: A consecutive sample of 17 children (13 girls). For 9 of them and their first-degree relatives, molecular analyses were performed in the K6HF gene with 50 appropriate controls. INTERVENTION: Minoxidil therapy (5% lotion) in 11 patients for 1 to 12 months. MAIN OUTCOME MEASURES: Clinical and follow-up features and determination of mutations in the K6HF gene.
RESULTS: Most patients had easily pluckable hair with no sign of scalp inflammation or scarring. Ten patients seldom cut their hair, and 4 had unmanageable hair. One patient had hypodontia. Two patients had an additional clinical phenotype of diffuse partial woolly hair. The family history was positive for loose anagen hair syndrome in 5 patients. Marked improvement was noted after treatment with 5% minoxidil lotion in 7 of the 11 patients treated. Polymerase chain reaction analysis of the gene segments encoding the alpha-helical 1A and 2B subdomains of K6hf, the type II cytokeratin exclusively expressed in the companion layer, was performed in 9 families. In 3 of these 9 families, a heterozygous glutamic acid and lysine mutation, E337K, was identified in the L2 linker region of K6HF.
CONCLUSIONS: Diffuse partial woolly hair can be associated with loose anagen hair syndrome. A keratin mutation, E337K in K6HF, was possibly causative in 3 of the 9 families studied. Another keratin, and possibly the type I partner of K6hf, could be responsible for loose anagen hair syndrome in other patients, or the gene involved may be a minor gene.

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Year:  2002        PMID: 11939812     DOI: 10.1001/archderm.138.4.501

Source DB:  PubMed          Journal:  Arch Dermatol        ISSN: 0003-987X


  13 in total

1.  Hopx expression defines a subset of multipotent hair follicle stem cells and a progenitor population primed to give rise to K6+ niche cells.

Authors:  Norifumi Takeda; Rajan Jain; Matthew R Leboeuf; Arun Padmanabhan; Qiaohong Wang; Li Li; Min Min Lu; Sarah E Millar; Jonathan A Epstein
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2.  Hair keratin mutations in tooth enamel increase dental decay risk.

Authors:  Olivier Duverger; Takahiro Ohara; John R Shaffer; Danielle Donahue; Patricia Zerfas; Andrew Dullnig; Christopher Crecelius; Elia Beniash; Mary L Marazita; Maria I Morasso
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3.  A small deletion hotspot in the type II keratin gene mK6irs1/Krt2-6g on mouse chromosome 15, a candidate for causing the wavy hair of the caracul (Ca) mutation.

Authors:  Yoshiaki Kikkawa; Ayumi Oyama; Rie Ishii; Ikuo Miura; Takashi Amano; Yoshiyuki Ishii; Yasuhiro Yoshikawa; Hiroshi Masuya; Shigeharu Wakana; Toshihiko Shiroishi; Choji Taya; Hiromichi Yonekawa
Journal:  Genetics       Date:  2003-10       Impact factor: 4.562

4.  Diffuse partial woolly hair in a patient with epidermolysis bullosa simplex with mottled pigmentation.

Authors:  Agnieszka Gerkowicz; Ralph M Trüeb
Journal:  Int J Trichology       Date:  2014-04

5.  The chicken frizzle feather is due to an α-keratin (KRT75) mutation that causes a defective rachis.

Authors:  Chen Siang Ng; Ping Wu; John Foley; Anne Foley; Merry-Lynn McDonald; Wen-Tau Juan; Chih-Jen Huang; Yu-Ting Lai; Wen-Sui Lo; Chih-Feng Chen; Suzanne M Leal; Huanmin Zhang; Randall B Widelitz; Pragna I Patel; Wen-Hsiung Li; Cheng-Ming Chuong
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6.  Loose anagen hair syndrome.

Authors:  Rachita P Dhurat; Deepal J Deshpande
Journal:  Int J Trichology       Date:  2010-07

7.  Light microscopy of the hair: a simple tool to "untangle" hair disorders.

Authors:  Keshavmurthy A Adya; Arun C Inamadar; Aparna Palit; Ragunatha Shivanna; Niranjan S Deshmukh
Journal:  Int J Trichology       Date:  2011-01

8.  Loose Anagen Hair Syndrome.

Authors:  Sahana M Srinivas
Journal:  Int J Trichology       Date:  2015 Jul-Sep

Review 9.  The human keratins: biology and pathology.

Authors:  Roland Moll; Markus Divo; Lutz Langbein
Journal:  Histochem Cell Biol       Date:  2008-05-07       Impact factor: 4.304

10.  Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75.

Authors:  Ying Liu; Elizabeth R Snedecor; Xu Zhang; Yanfeng Xu; Lan Huang; Evan C Jones; Lianfeng Zhang; Richard A Clark; Dennis R Roop; Chuan Qin; Jiang Chen
Journal:  J Invest Dermatol       Date:  2016-01       Impact factor: 8.551

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