Results 51 to 60 of about 14,321 (288)
Medicina, 2022 Background and Objectives: We aimed to analyze and compare the outcomes of conventional ectropion surgery procedures with and without concurrent bicanalicular nasolacrimal duct intubation to identify if the combination of procedures could serve as a ...
Anthia Papazoglou +4 more
doaj +1 more source
Expanding the Clinical and Genetic Spectrum of KRT1, KRT2 and KRT10 Mutations in Keratinopathic Ichthyosis [PDF]
, 2016 Twenty-six families with keratinopathic ichthyoses (epidermolytic ichthyosis, superficial epidermolytic ichthyosis or congenital reticular ichthyosiform erythroderma) were studied.
Betz, Regina C. +12 more
core +2 more sources
Bladder Eversion Through a Vesicovaginal Fistula in a Patient With Complete Uterine Prolapse
IJU Case Reports, EarlyView.ABSTRACT Introduction We report a case of bladder eversion through a vesicovaginal fistula (VVF) in an elderly patient with severe pelvic organ prolapse (POP). Case Presentation A 90‐year‐old woman presented with a sensation of prolapse and urinary leakage.
Ryoken Tsunekawa +6 more
wiley +1 more source
Veterinary Record Case Reports, EarlyView.Abstract Homozygous sauteur d'Alfort rabbits have a splicing‐site mutation in the RAR‐related orphan receptor B (RORB) gene that causes changes in their locomotion. These rabbits sometimes walk on their thoracic limbs, especially at higher speeds. They also experience additional abnormalities, including eye alterations such as blindness due to retinal ...
Kerstin Müller +4 more
wiley +1 more source
Síndrome da frouxidão palpebral: revisão da literatura [PDF]
, 2011 Floppy eyelid syndrome is characterized by the easy evertion of the upper eyelid which occurs spontaneously during the sleep, causing the exposure of the eye surface and chronic papillary conjunctivitis. Its pathogenesis is not totally defined yet: it is
Cariello, Angelino Julio +5 more
core +3 more sources
The Phenotypic Spectrum of Miller Syndrome: Insight From a French Cohort
Clinical Genetics, EarlyView.This study expands the clinical spectrum of Miller syndrome by reporting novel features including preaxial defects, facial nevus simplex, and optic atrophy. It also includes the first patients with homozygous DHODH variants, emphasizing the importance of early diagnosis and the variability of presentations, from severe prenatal to mild adult phenotypes.
Marion Aubert Mucca +13 more
wiley +1 more source
Progressive ectropion uveae and secondary angle-closure glaucoma in type 1 neurofibromatosis
American Journal of Ophthalmology Case Reports, 2022 Purpose: To present a case of progressive ectropion uveae and secondary angle-closure glaucoma in association with type 1 neurofibromatosis (NF-1). Observation: An 11-year-old-Hispanic-male with a known history of NF-1 who was followed for the ocular ...
Hamed Esfandiari +2 more
doaj
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
Correction of Cicatricial Upper Eyelid Ectropion Using a Dermofat Graft and an Anti-Adhesive Agent [PDF]
Archives of Aesthetic Plastic Surgery, 2018 Ectropion is characterized by eversion of the eyelid margin and exposure of the cornea and conjunctiva. This leaves the inner eyelid surface exposed and prone to irritation, and in severe cases, poor eye closure.
Suk Yoon Jang +3 more
doaj +1 more source
Obstetrical aspects in congenital ichtyosis [PDF]
, 2016 We present a case of congenital ichthyosis because obstetrical literature is scarce and most obstetricians could need a reminder and update. Congenital ichthyosis (CI) comprises a variety of skin disorders characterised by abnormal keratinization of the ...
Dehaene, Isabelle +2 more
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