Results 91 to 100 of about 5,567,486 (203)
Clinical Presentation of Ocular Surface Squamous Neoplasia in Kenya. [PDF]
, 2015 IMPORTANCE: There is a trend toward treating conjunctival lesions suspected to be ocular surface squamous neoplasia (OSSN) based on the clinical impression.
Burton, Matthew J +12 more
core +1 more source
Expanding the Clinical Spectrum of Bruck Syndrome: A Case Report and Literature Review
Case Reports in Pediatrics, Volume 2026, Issue 1, 2026.Background Bruck syndrome is a rare autosomal recessive disorder characterized by osteogenesis imperfecta–like bone fragility and congenital joint contractures. Clinical overlap with other connective tissue disorders makes early diagnosis challenging, and genetic testing remains essential.
Ansam Nafah +5 more
wiley +1 more source
Conjunctival Limbal Autograft Implantation in Primary and Recurrent Pterygium
Beyoglu Eye Journal, 2018 INTRODUCTION[|]The aim of this study was to evaluate the clinical results and recurrence rate after pterygium excision with a conjunctival limbal autograft in patients with primary and recurrent pterygium.[¤]METHODS[|]Patients who had primary (Group 1 ...
Ali Demircan
doaj +1 more source
Effects of Different Types of Primary Pterygium on Changes in Oculovisual Function
, 2020 Pterygium are known to cause reduction in oculovisual function. However, the effects are varying due to its various morphological factors, thus, the impact on patient are difficult to predict which indirectly not all pterygium need to be excised.
M. Hilmi +9 more
semanticscholar +1 more source
Awareness of treatment: a source of bias in subjective grading of ocular complications [PDF]
, 2019 Purpose: Bias has been described as one important obstacle in scientific research. The aim of this study was to explore “awareness of treatment” as a possible source of bias in subjective grading of ocular complications.
Cardona Torradeflot, Genís +1 more
core +2 more sources
Clinical Case Reports, Volume 13, Issue 12, December 2025.ABSTRACT Congenital syngnathia, the rare fusion of the maxilla and mandible, poses significant feeding and respiratory challenges. Its management is complicated by rarity and potential syndromic associations. We present a 1‐week‐old female neonate who presented with left jaw deviation, respiratory distress (SpO2 69%, tachypnea), and fever.
Asteway M. Haile +5 more
wiley +1 more source
Matrix Metalloproteinases and Glaucoma Treatment. [PDF]
, 2020 Matrix metalloproteinases (MMPs) are a family of proteolytic enzymes that degrade extracellular matrix (ECM) components such as collagen and have important roles in multiple biological processes, including development and tissue remodeling, both in ...
Dibas, Mohammed +3 more
core
Amniotic membrane transplantation [PDF]
, 2000 Amniotic membrane transplantation has been used as an alternative for ocular surface reconstruction. Indications for amniotic membrane transplantation include persistent epithelial defects, pterygium, Stevens-Johnson syndrome, ocular cicatricial ...
Moreira, Hamilton +1 more
core +2 more sources
Med Research, Volume 2, Issue 1, Page 190-194, March 2026.
Benjamin Abaidoo +6 more
wiley +1 more source
American Journal of Medical Genetics Part A, Volume 197, Issue 11, November 2025.ABSTRACT Neuroaxonal dystrophy (NAD) with osteopetrosis syndrome (OMIM # 600329) was first reported in a consanguineous Moroccan Jewish family. However, to date, no genetic variant has been linked to this disease. We report on sibs, born to consanguineous Pakistani parents identified prenatally with cerebral ventriculomegaly and agenesis of the corpus ...
Yael Fisher +6 more
wiley +1 more source