Hair: more than just an appendage

Authors

  • Harshitha Reddy Department of Dermatology, Venerology and Leprology, Mahatma Gandhi Medical College and Research Institute, Pondicherry, India
  • Srikanth Shanmugam Department of Dermatology, Venerology and Leprology, Mahatma Gandhi Medical College and Research Institute, Pondicherry, India
  • Manobalan Karunanandhan Department of Dermatology, Venerology and Leprology, Mahatma Gandhi Medical College and Research Institute, Pondicherry, India

DOI:

https://doi.org/10.18203/issn.2455-4529.IntJResDermatol20212559

Keywords:

Hypotrichosis, Hereditary hypotrichosis simplex, Ectodermal defects, Trichoscopy

Abstract

Hypotrichosis is a relatively common feature of a number of complex hereditary syndromes. However, the isolated variant, called hereditary hypotrichosis simplex (HHS), is uncommon. We present a 4 years old child and his father who presented to us with features suggestive of HHS. No other associated ectodermal and systemic abnormalities were noted.

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Author Biography

Srikanth Shanmugam, Department of Dermatology, Venerology and Leprology, Mahatma Gandhi Medical College and Research Institute, Pondicherry, India

Professor, Department of Dermatology, Venereology and Leprosy

Mahatma Gandhi Medical College and Research Institute, Pondicherry

References

Cruz CF, Costa C, Gomes AC, Matamá T, Cavaco-Paulo A. Human Hair and the Impact of Cosmetic Procedures: A Review on Cleansing and Shape-Modulating Cosmetics. Cosmetics. 2016;3(3):20-6.

Koslu A, Ekmekci TR, Cetincelik U. A case of hereditary hypotrichosis simplex. J Eur Acad Dermatol Venereol. 2006;20(9):1150-1.

Pasricha JS, D’Souza P. Topical fluocinolone acetonide acetate ointment in autosomal dominant congenital hypotrichosis. Indian J Dermatol Venereol Leprol. 1996;62(4):242-5.

Farah RS, Holahan HM, Moye MS, Stone MS, Swick BL. Hereditary Hypotrichosis Simplex of the Scalp. 2017;100(1):12-4.

Moravvej-Farshi H, Ayatollahi A, Hejazi S. Hereditary hypotrichosis simplex of the scalp. Indian J Dermatol. 2014;59(6):634.

Li M, Cheng R, Zhuang Y, Yao Z. A recurrent mutation in the APCDD1 gene responsible for hereditary hypotrichosis simplex in a large Chinese family. Br J Dermatol. 2012;167(4):952-4.

Vázquez MR, Rodríguez RR, Tapia AG, Diez LI. Hereditary Hypotrichosis Simplex of the Scalp. Pediatr Dermatol. 2002;19(2):148-50.

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Published

2021-06-24

Issue

Section

Case Reports