Results 51 to 60 of about 10,708 (219)
Bullous aplasia cutis congenita: A report of two cases and brief review of the selected literature [PDF]
Vojnosanitetski Pregled, 2019 Introduction. Aplasia cutis congenita (ACC) is a rare condition characterized by the focal absence of skin, and sometimes other underlying structures at birth. It may occur as an isolated defect or associated with other anomalies and defects. Bullous ACC
Prćić Sonja +5 more
doaj +1 more source
, 2018 Zusammenfassung: Hypertrichose bezeichnet, auf Lokalisation, Alter, Geschlecht und ethnische Provenienz bezogen, übermäßiges, diffuses oder umschriebenes Haarwachstum, das nicht dem Verteilungsmuster der sekundären männlichen Geschlechtsbehaarung ...
Trüeb, R.M.
core
Prevalence of Becker Nevus in Young Men [PDF]
, 2013 Background and Design: Becker nevus (BN), characterized by sharply and irregularly bordered, unilaterally localized, hyperpigmented macules and patches which can go along with hypertrichosis, is a kind of hamartomatous lesion that predominantly affects ...
Bilal Doğan +3 more
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Kaposiform hemangioendothelioma: Diagnosis and treatment
Pediatric Investigation, EarlyView.Vascular endothelial growth factor‐C (VEGF‐C)/vascular endothelial growth factor receptor‐3 (VEGFR‐3) and angiopoietin‐2 (Ang‐2)/tyrosine kinase with immunoglobulin‐like and EGF‐like domain 2 (TIE2) signaling pathways play an important role in lymphangiogenesis.
Yi Tian +5 more
wiley +1 more source
Gingival fibromatosis with hypertrichosis syndrome: Case series of rare syndrome
Indian Journal of Dental Research, 2017 Gingival fibromatosis with hypertrichosis syndrome is an extremely rare genetic condition characterized by profound overgrowth of hair and gums, as well as other variable features.
Preetha Balaji, S M Balaji
doaj +1 more source
Facial hypertrichosis after isotretinoin therapy: Is it a side effect or coincidence?
Turkderm Turkish Archives of Dermatology and Venereology, 2022 Background and Design: Excessive hair growth after isotretinoin treatment for acne vulgaris is not common, but may be one of the most undesirable side effects of the drug.
Esra Saraç, Alkım Ünal
doaj +1 more source
The phenotypic and genotypic spectra of ichthyosis with confetti plus novel genetic variation in the 3' end of KRT10: from disease to a syndrome [PDF]
, 2015 Ichthyosis with confetti (IWC) is a genodermatosis caused by dominant negative mutations in the gene encoding keratin 10 (KRT10). We investigated clinical and genetic details of a substantial number of patients with IWC in order to define major and minor
Brena, Michela +7 more
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Clinical Genetics, EarlyView.This study expands the clinical spectrum of SMARCA4 by describing a novel phenotype in three unrelated individuals with truncating variants. Distinct from Coffin–Siris syndrome and rhabdoid tumor predisposition, this new association is characterized by ocular malformations, specifically microphthalmia and coloboma.
Bertrand Chesneau +7 more
wiley +1 more source
Barber Say Syndrome (A new case report)
Indian Dermatology Online Journal, 2019 Barber Say syndrome (BSS) is a rare ectodermal dysplasia with neonatal onset characterized by congenital generalized hypertrichosis, atrophic skin, ectropion and macrostomia. A literature review showed less than 20 previously reported cases of Barber Say
Mehrdad Rezaei +2 more
doaj +1 more source
Veterinary Sciences, 2022 Poor recognition of subtle clinical abnormalities and equivocal ACTH concentrations make early diagnosis of PPID difficult. Progressive clinical findings and corresponding ACTH concentrations in horses transitioning to PPID over time have not been ...
Naomi C. Kirkwood +2 more
doaj +1 more source