Results 171 to 180 of about 51,514 (235)

Alopecia Universalis in a Horse

Veterinary Dermatology, 1994
Abstract— Alopecia universalis was diagnosed in a 3‐year‐old brown Percheron mare. Clinical and histo‐pathologic findings in this previously unreported condition in the horse are described.
Deborah J, Middleton, Sally, Church
openaire   +2 more sources

Alopecia areata universalis in an infant

Journal of Cutaneous Medicine and Surgery, 2001
Background: Alopecia areata (AA) is common during childhood and rarely reported in infants. The four reported cases of AA in infants all exhibited circumscribed patches of alopecia that appeared at birth or shortly thereafter. Objective: We report a case of alopecia areata universalis that developed after birth along with fingernail changes of ...
J A, LaRow, J, Mysliborski, I P, Rappaport, G A, Rouleau, J A, Carlson   +4 more
openaire   +2 more sources

Resolution of Alopecia Universalis After Initiation of Hemodialysis - A Case Report

Indian Journal of Nephrology
A 49-year-old male with CKD secondary to chronic interstitial nephritis developed alopecia universalis (AU), characterized by complete loss of scalp, facial, and body hair. Laboratory tests ruled out autoimmune or nutritional causes.
Sagar Hase, Ravi Sarvi, Mallikarjun Karishetti   +2 more
semanticscholar   +1 more source

Down Syndrome, Alopecia Universalis, and Trachyonychia

Pediatric Dermatology, 1993
Abstract: A 16‐year‐old boy with Down syndrome and alopecia universalis had dystrophy of all nalis. A presumptive diagnosis of tinea ungulum, common in persons with Down syndrome, had been made nine years earlier. Despite antifungal therapy, the condition of the nails worsened. We were unable to detect fungi, and believe that his nail changes are most
S A, Norton, C W, Demidovich
openaire   +2 more sources

Sintilimab-induced Alopecia Universalis in a Patient With the Anti-tumor Effect of Complete Remission After Hepatectomy

Journal of immunotherapy, 2023
Immune checkpoint blockades have been widely used to treat various malignancies. Programmed cell death protein 1 (PD-1) inhibitor-induced alopecia areata, one of the immune-related adverse events, is rarely reported.
Liang Wen, Jianhui Zhao, Yi-xin Yang, Wen Chen, Ying-Xiao Bao, Jian Zhang, T. Wei, Lijuan Zhou, Bin Xi, Yun Zhang, T. Liang   +10 more
semanticscholar   +1 more source

Alopecia Universalis, Onychodystrophy, and Total Vitiligo

Archives of Dermatology, 1963
Two patients with the syndrome of alopecia universalis, onychodystrophy, and apparent total vitiligo are reported. Extensive investigations including endocrinologic evaluation and viral cultures failed to reveal a systemic abnormality or evidence of an etiologic agent.
D J, DEMIS, M A, WEINER
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Review of treatment for alopecia totalis and alopecia universalis

International Journal of Dermatology, 2017
AbstractAlopecia areata (AA) is an autoimmune disease directed at the hair follicle. Although usually limited to patchy hair loss over the scalp (focalis), AA can present as total loss of scalp hair (totalis; AT) or as total loss of both scalp and body hair (universalis; AU).
Sama, Kassira, Dorota Z, Korta, Lance W, Chapman, Francis, Dann   +3 more
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Management of Pediatric Alopecia Universalis through Ayurveda: An experience

Journal of Ayurveda Case Reports
Alopecia Areata (AA) is an autoimmune disorder of the hair follicle characterized by nonscarring scalp hair loss. Alopecia Universalis (AU) is a severe form of AA with more extensive hair loss from various parts of the body.
Emy S. Surendran, Praveen Balakrishnan, Archana Sivan, Subhose Varanasi   +3 more
semanticscholar   +1 more source

Successful management of therapy-resistant chronic refractory atopic dermatitis and alopecia universalis with oral tofacitinib in a girl.

International Journal of Risk and Safety in Medicine
BackgroundThe association between alopecia areata (AA) and atopic dermatitis (AD) is common. The association of both autoimmune diseases is an indicator of poor prognosis.
Shreya K. Gowda, Bhini Ameta, Akash Agarwal, B. Behera   +3 more
semanticscholar   +1 more source

Congenital alopecia universalis.

The Journal of the Association of Physicians of India, 1990
A case of congenital alopecia universalis without any other ectodermal defect and mental abnormality is described in a girl of eight years. There was no family history in any of the members. The child was born of a non-consanguineous marriage.
P K, Saraswat, N N, Laha
openaire   +1 more source