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types of hair fiber

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Types of hair fiber/follicle

Many hair subtypes have been classified in other species. For example, in adult rodents hair types can be classified into vibrissa, guard, awl, auchene, and peri-anal hairs. There are several different types of hair follicle present in humans that are distinct from hair types found in other species. Although the basic human hair follicle structure remains the same, the type of fiber that is produced can be quite different. More than one hair type can be made by the same hair follicle at different times. Humans have several different types of hair that can be classified depending on their body position and form. Size, angle of penetrance through the skin, embryological time of first appearance, and structural variations in the hair follicles are all taken into account when classifying hair types.

Dermatologists working on embryology or pediatric development of hair with age describe three different hair types, primary, secondary, and tertiary hair. The categories are based on the length and diameter of the hair follicles in the skin. Primary hair is the hair type produced in the very first cycle of hair growth that a hair follicle enters shortly after it develops in the embryo. Primary hair is also correctly described as lanugo hair. During the first year of life hair follicles go through significant structural changes. The secondary or vellus hair gradually replaces the primary hair and depending on position of the body where the hair follicles are present, the vellus hair may turn to tertiary or terminal hair.

Another classification system can be made based on the active response of hair follicles towards steroidal hormones. Many hair follicles take little notice of the general levels of hormones those follicles of the eyebrows, lashes, and extremities of the hands and feet are generally consistent in their production of fiber regardless of hormone concentration in males and females. A second category would include hair follicles responsive to female hormone levels (low androgen concentration). These hair follicles are generally limited to the pubic and arm pit areas plus some hair follicles on the limbs and chest. A third category would include those hair follicles responsive to male concentrations of androgen hormones. Hair regions would include the beard and mustache, nasal hair, beard hair, upper back hair, chest hair, and scalp vertex hair.

Essentially, there are three basic groups of hair based on hair follicle size.

A) Lanugo. Lanugo hair is the very first hair fiber to be produced by a hair follicle. As an embryo develops in the womb the hair follicles form and begin to produce this type of hair. Lanugo hair is long, unpigmented and very fine. This first wave of hair growth is normally shed by the embryo at around 8 months gestation while in the womb and replaced by terminal or vellus hair ready for birth. However, sometimes babies can be born with this coat of lanugo hair. This rare condition is called "congenital hypertrichosis lanuginosa".

B) Vellus. Vellus hair is short fine unpigmented hair. It is the fuzzy hair found on the nose and over the cheeks. It is some times incorrectly referred to as lanugo hair. Sometimes vellus hair can grow exceptionally long particularly in people with malignancies. This excessively long vellus hair is defined as the disease "acquired hypertrichosis lanuginosa". Strictly speaking long vellus hair is not lanugo hair despite the disease name.

C) Terminal. Terminal hair comes from large hair follicles. It is long, coarse, pigmented and frequently contains a medulla. A hair follicle is capable of switching from vellus hair production to terminal hair and switching back again. During puberty many hair follicles around the genitals, arm pits, beard and chest in men transform from vellus hair to terminal hair under the direction of hormones. Equally hormones can cause terminal hairs to revert to vellus hair production as in androgenetic alopecia.

In adults hair exists in a variety of locations, patterns, and density over the body. Terminal hairs can be further subdivided into different types depending on their nature and/or position of growth on the body. The hair characteristics are genetically determined within each follicle. Different terminal hair types include;

1) Eyebrow hair. Eyebrow hair is a protective patch of hair above the eye sockets. It channels away sweat and other fluids and helps reduce any excessive glare from sunlight entering the eyes. Average maximum hair length is about 10mm. The hair fiber is curved and coarse and includes a medulla. Hair growth rate is typically 0.16mm per day in both men and women. This is one of the slowest growth rates of any hair follicle type found on the human body. Slow growth has led to some degree of superstition from many in the medical and cosmetic industries. Some surgeons are wary of shaving eyebrows for fear they will not grow back. They do grow but the rate of growth is so slow that the patient may become concerned. Eyebrow follicles are also sensitive to injury. Plucking an eyebrow follicle once or twice may lead to extensive and irreversible destruction and no further hair growth.

2) Eyelash hair. Eyelash hair is very similar to eyebrow hair. Average length is around 7.5mm and the growth rate is about the same as for eyebrows. Eyelashes are very important in protecting the eye from dust and debris. People without eyelashes have frequent problems with eye contamination and a possible increase in eye infection that requires regular attention from an ophthalmologist.

3) Scalp hair. Scalp hair is terminal hair unless the hair follicles have been affected by disease such as androgenetic alopecia. Terminal scalp hair grows in a clockwise whorl pattern on the top of the head with merging of this pattern into hair angled downwards and away from the face around the ears and lower back of the scalp. Growth rates are up to 0.35mm per day, possibly slightly faster in females (0.36mm) than males (0.34mm).

4) Beard hair. The beard develops in response to testosterone/steroidal hormones during puberty. These hair follicles produce thick, coarse, terminal hair. The hair follicles are some of the fastest producers of hair with a mean growth rate around 0.38mm per day.

5) Body hair. Some hairs on the arms legs and torso are mildly responsive to androgens. Other neighboring follicles may not have androgen receptors. This distinction leads to some body hair follicles producing pigmented terminal hair in response to androgen stimulation in adulthood when neighboring follicles continue to produce vellus hair.

6) Whisker hair. The hair follicles on the chin are highly androgen responsive in both men and women. Women with abnormally high androgen levels can grow beards. Note that whiskers are not the same as the vibrissae on rodents and cats. Vibrissae are specially modified follicles with numerous sensory nerve endings in an around the hair follicle structure to detect movement in the hair fiber.

7) Pubic hair. Pubic hair is a kind of terminal hair type. It is usually pigmented and of large diameter. The kinks in it make its appearance distinctive.

8) Peri-anal hair. Not much is known about peri-anal hairs, I guess because no researcher wants to poke around down there! They are terminal hairs and, as the name suggests, they surround the anus. Peri-anal hairs are distinguished from other hair types in the vicinity by their size and their unusually large associated sebaceous glands. Peri-anal hairs apparently produce a lot of oil if the size of the sebaceous glands are anything to go by.


Types of hair fiber/follicle references

  • Hess WM, Seegmiller RE, Gardner JS, Allen JV, Barendregt S. Human hair morphology: a scanning electron microscopy study on a male Caucasoid and a computerized classification of regional differences. Scanning Microsc. 1990 Jun;4(2):375-86.
  • Hutchinson PE, Thompson JR. The cross-sectional size and shape of human terminal scalp hair. Br J Dermatol. 1997 Feb;136(2):159-65.
  • Barbareschi M, Sibillo E, Greppi F, Bruscagin C, Crosti C. "Twisted and rolled body hairs": an ultrastructural study by means of scanning electron microscopy. Acta Derm Venereol. 1997 Sep;77(5):409-10.
  • Alcaraz MV, Villena A, Perez de Vargas I. Quantitative study of the human hair follicle in normal scalp and androgenetic alopecia. J Cutan Pathol. 1993 Aug;20(4):344-9.
  • Corcuff P, Roguet R, Kermici M. A method for measuring the various constituents of the human hair follicle. J Microsc. 1989 Oct;156 ( Pt 1):115-23.
  • Lindelof B, Forslind B, Hedblad MA, Kaveus U. Human hair form. Morphology revealed by light and scanning electron microscopy and computer aided three-dimensional reconstruction. Arch Dermatol. 1988 Sep;124(9):1359-63.
  • Headington JT. Transverse microscopic anatomy of the human scalp. A basis for a morphometric approach to disorders of the hair follicle. Arch Dermatol. 1984 Apr;120(4):449-56.
  • Pacini P, Zecchi S, Orlandini GE. [Statistical findings on scalp hair as observed by scanning electron microscopy] Boll Soc Ital Biol Sper. 1983 May 30;59(5):603-7.
  • Bonelli A, Pacini P. [Scanning electron microscopy of human hairs of subjects of different age and sex] Arch Ital Anat Embriol. 1980;85(2):179-87.
  • Bhatia RY, Rao KV, Rao NP. Site variations in scalp hair morphology in pre-school children. Indian J Med Res. 1980 Jun;71:890-2.
  • Wyatt EH, Riggott JM. Scanning electron microscopy of hair. Observations on surface morphology with respect to site, sex and age in man. Br J Dermatol. 1977 Jun;96(6):627-33.
  • Bottoms E, Wyatt E, Comaish S. Progressive changes in cuticular pattern along the shafts of human hair as seen by scanning electron microscopy. Br J Dermatol. 1972 Apr;86(4):379-84.
  • Dawber R, Comaish S. Scanning electron microscopy of normal and abnormal hair shafts. Arch Dermatol. 1970 Mar;101(3):316-22.
  • Sims RT, Knollmeyer HH. Multivariate normal frequency distributions for the analysis of scalp hair measurements. Br J Dermatol. 1970 Jul;83(1):200-7.
  • Caputo R, Ceccarelli B. Study of normal hair and of some malformations with a scanning electron microscope. Arch Klin Exp Dermatol. 1969;234(3):242-9.

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