|Year : 2015 | Volume
| Issue : 5 | Page : 352-353
Chandraprakash Chouhan, Rajeev Khullar, Pankaj Rao, Ramesh Raidas
Departments of Dermatology, Venereology and Leprosy, Dr. SN Medical College, Jodhpur, Rajasthan, India
|Date of Web Publication||4-Sep-2015|
Department of Dermatology, F-46, UIT Colony Pratap Nagar, Jodhpur - 342 004, Rajasthan
Source of Support: Nil, Conflict of Interest: None declared.
| Abstract|| |
Atrichia congenita is a rare genodermatoses is characterized by a mutation of the human hairless (HR) gene on chromosome 8p22. There is loss of scalp hair between one to six months of age, after which no growth occurs. Eyebrow, eyelash, and body hair may also be sparse or absent; patients may have a few pubic and axillary hairs. The condition may present in isolation or along with other defects.
Keywords: Atrichia Congenita, autosomal recessive, human hairless gene, loss of scalp hair
|How to cite this article:|
Chouhan C, Khullar R, Rao P, Raidas R. Atrichia congenita. Indian Dermatol Online J 2015;6:352-3
| Introduction|| |
Atrichia congenita without ectodermal defects (isolated form) is a rare autosomal recessive condition characterized by the shedding of scalp hairs between one and six months of age, after which no growth occurs. Eyebrow, eyelash and body hair may also be sparse or absent; patients may have a few pubic and axillary hairs. It may occur either in isolation or with associated defects. Isolated congenital alopecia has been reported to occur in both sporadic and familial forms. In the isolated familial form, inheritance is usually autosomal recessive, although dominant or irregular dominant inheritance has occurred in some families., The gene locus for familial cases is on chromosome 8p21-22 (ALUNC-Alopecia Universalis Congenitalis), and mutation of the human hairless (HR) gene on chromosome 8p21-22 produces the clinical picture of atrichia congenita., Human HR gene is a homologue of the murine hairless gene,, and encodes a zinc-finger transcription factor protein that is expressed in the brain and the skin.
| Case Report|| |
A one-and-a-half-month-old male baby was brought by his maternal grandmother with complaints of frontoparietal scalp hair recession, sparse eyelashes and eyebrows [Figure 1]. The grandmother as well as two of her siblings (one female and one male) all had absent scalp, facial, axillary, and pubic hair since infancy. All three had normal hair growth at birth that shed within a few months. Two other siblings had normal hair. Their condition was unresponsive to steroid therapy. Physical growth was normal. Teeth, nail, mucosa, palms, and soles were normal. There was no bony abnormality or any systemic involvement. Examination revealed complete absence of scalp, facial, axillary, and pubic hair with no papular skin lesions. There was no visible perifollicular inflammation. Serum Vitamin D3 level and calcium were normal. Radiographs of the wrist joint were normal.
|Figure 1: Three siblings (two females and one male) with absence of scalp, facial, pubic and axillary hair, along with the maternal grandson (one-and-a-half-months) having frontoparietal recession, sparse eyelashes and eyebrows|
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There was no history of delayed milestones in the baby, hypohidrosis, bone pain, hearing loss, or seizures. Examination revealed frontoparietal scalp hair recession, with sparse eyelashes and eyebrows. The baby was otherwise normal.
| Discussion|| |
Atrichia congenita (isolated form) is a rare autosomal recessive form of alopecia. Patients are born with hair that falls and is never replaced. The condition may be confused with congenital alopecia universalis, vitamin D dependant rickets, and ectodermal dysplasia. In our patients, congenital alopecia universalis was ruled out on the basis of lack of any history of sudden, patchy loss of normally appearing hair progressing to the loss of scalp, body, eyelash, andv eyebrow hair. Vitamin D dependent rickets was ruled out on the basis of lack of any history of joint pain, normal serum vitamin D3 and calcium levels, and a normal wrist joint radiograph. Ectodermal dysplasia was excluded as there was no history of delayed milestones or loss of sweating. Teeth, nails, mucosa (ectodermal components), palms, and soles were normal. The presence of a family history, history of consanguinity, and sparse eyebrows and eyelashes at the time of birth pointed to the diagnosis of atrichia congenita.
Zlotogorski et al. proposed diagnostic criteria for atrichia congenita with papular lesions but later Yip et al. revised them [Table 1]. Our patients met two out of five major criteria supplemented by four minor criteria for the diagnosis of atrichia congenita (isolated form).
|Table 1: Diagnostic criteria for atrichia congenita with papular lesions|
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The case is being reported for its rarity.
| References|| |
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