Results 1 to 10 of about 8,391 (147)
Paediatric Hypotrichosis: A Clinical and Algorithmic Approach to Diagnosis. [PDF]
Australas J DermatolABSTRACT Paediatric hypotrichosis is the clinical feature of paucity of hair arising congenitally or in early life with the presentation being that of the child whose hair is growing insufficiently. It is a hallmark finding of a diverse group of genodermatoses and sporadic disorders, presenting as either an isolated symptom or in association with ...
So N, Yip L, Orchard D.
europepmc +2 more sources
The phenotypic spectrum of the Cornelia de Lange‐like “Alazami‐Yuan syndrome”: A case report of the 7th diagnosed individual and review of the literature [PDF]
Clin Case RepKey Clinical Message We present a 17‐year‐old female with a childhood clinical diagnosis of Cornelia de Lange Syndrome (CdLS), however later genetic testing identified compound heterozygous variants in TAF6, consistent with AYS. This case report adds to the phenotypic spectrum observed in AYS, and draws connections to transcriptional pathways between ...
Pappas A +6 more
europepmc +2 more sources
Pthiriasis of the eyelashes [PDF]
Giornale Italiano di Dermatologia e Venereologia, 2020 Pthirus pubis, popularly known as crab louse, usually infests the pubis, groin, buttocks, intergluteal fold and perianal region. However, it can also infest, in particular in hairy males or when the infestation is longstanding, the thighs, abdomen, chest, axillae and face. The involvement of the scalp is very rare. Eyelashes may also be involved.
Veraldi, Stefano +5 more
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The Journal of Pediatrics, 2019 A 27-month-old boy was referred to pediatric dermatology for the evaluation of crusts on his eyelashes; they had been present for 2 months and were increasing in number. The crusts had appeared after a trip to Bulgaria, where his family had been sleeping in several different hotels and places.
Ouedraogo, Muriel +4 more
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Indian Journal of Dermatology, 2015 Eyelash trichomegaly is increased length, curling, pigmentation or thickness of eyelashes. Various causes include congenital syndromes, acquired conditions and drugs. It can manifest at birth or present later in life. It can form a part of spectrum of manifestations of some congenital syndromes. Although it tends to have a benign course, it can lead to
Sandeep Kaur, Bharat Bhushan Mahajan
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A closer look at the eyelashes!
Pan African Medical Journal, 2019 A 7-year-old child presented with bilateral anterior blepharitis. He had no medical history. The careful examination of the eyelashes found several lice attached to them with their ovoid nits. The parasitological examination revealed a phtirius pubis. Screening of other family members did not find similar effects. The treatment consisted in the removal
O. Cherkaoui, Kawtar Belkhadir
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Seminars in Plastic Surgery, 2007 Loss of eyelashes may occur with several conditions, including a variety of skin diseases, drug side effects, endocrine disorders, metabolic abnormalities, traumatic insults, inflammations, toxins, psychiatric disorders, and systemic disease. If the history and results of clinical, laboratory, and consultative assessments are negative, one must ...
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Eyelash transplantation for the treatment of vitiligo associated eyelash leucotrichia
Journal of Cutaneous and Aesthetic Surgery, 2016 Eyelash leucotrichia is cosmetically disfiguring condition and remains a therapeutic challenge in successful management of vitiligo.To study the efficacy of eyelash transplantation in management of eyelash leucotrichia associated with vitiligo.Fifteen patients with eyelash leucotrichia were treated with follicular unit transplantation.
Shekhar Neema +3 more
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Advanced Sensor Research, EarlyView.A wearable capacitive eye tracker for chronic fatigue assessment is presented, utilizing cylindrically shaped capacitive sensors made of a carbon nanotube‐paper composite. By integrating a novel fatigue‐induction protocol with machine learning, the device achieves 0.75‐sensitivity and 0.73‐specificity, providing a practical alternative to existing ...
Tianyi Li +6 more
wiley +1 more source
A New EP300‐Related Syndrome With Prominent Developmental and Immune Phenotypes
American Journal of Medical Genetics Part A, EarlyView.ABSTRACT Rubinstein Taybi syndrome (RTS) is a disorder of chromatin remodeling and transcriptional regulation caused by heterozygous pathogenic variants in CREBBP and EP300. RTS is characterized by a distinct facial gestalt, intellectual disability, structural kidney and heart differences, feeding difficulties, and broad thumbs and great toes ...
Devi Priyanka Maripuri +3 more
wiley +1 more source