Results 91 to 100 of about 631,158 (216)

Hepatoblastoma in a patient with Goldenhar Syndrome [PDF]

open access: yes, 2023
Goldenhar Syndrome (GS), also known as oculo-auricular vertebral syndrome, is a congenital defect that occurs in 1 of 5,000 births characterized by the underdevelopment of the ears, soft palate, lip, and mandible due to an anomaly of the first and second
Akhtar, Samina   +3 more
core   +1 more source

Contiguous diastematomyelia with tethered cord, intradural extramedullary dermoid tumor, and lipomyelomeningocele: A unique case of spinal dysraphism

open access: yesClinical Case Reports, Volume 12, Issue 4, April 2024.
Key Clinical Message Diastematomyelia, tethered cord, intradural extramedullary dermoid tumor and lipomyelomeningocele such disease entities themselves are rare in their own form and concurrent presentation of all those pathological states in a single individual can be considered one of the rarest forms of spinal dysraphism globally.
Sagun Ghimire   +7 more
wiley   +1 more source

Combination therapy of low-fluence photodynamic therapy and intravitreal ranibizumab for choroidal neovascular membrane in choroidal osteoma

open access: yesIndian Journal of Ophthalmology, 2011
Choroidal osteoma is an unusual form of intraocular calcification seen in otherwise healthy eyes. It is a benign idiopathic osseous tumor of the choroid, typically seen in young females. Choroidal neovascular membrane (CNVM) is a complication seen in one-
Rodney J Morris   +3 more
doaj   +1 more source

Corneal Diseases in Children in The Gambia [PDF]

open access: yes, 2009
Background: Blindness surveys carried out in The Gambia in 1986 reported childhood blindness from non-trachomatous corneal diseases as the commonest cause of blindness in children. The major causes were, post measles keratopathy, vitamin A deficiency and
Ceesay, W, Iwuora, NA, Onabolu, ROO
core   +2 more sources

An Infant With Congenital Scalp, Nail, and Limb Anomalies

open access: yes
Pediatric Dermatology, Volume 42, Issue 2, Page 407-409, March/April 2025.
Sabrina Yang, Joseph M. Lam
wiley   +1 more source

Atypical mandibulofacial dysostosis with microcephaly diagnosed through the identification of a novel pathogenic mutation in EFTUD2

open access: yesMolecular Genetics &Genomic Medicine, Volume 12, Issue 4, April 2024.
This study reported an untypical patient with mandibulofacial dysostosis with microcephaly (MFDM), who exhibited previously unreported phenotypes, including orbit anomalies and spina bifida occulta. A novel pathogenic insertion mutation of EFTUD2 was identified by whole‐exome sequencing as the etiology for this MFDM case, highlighting the importance of
Ying Chen   +9 more
wiley   +1 more source

Nasopalpebral lipoma coloboma syndrome

open access: yesIndian Journal of Ophthalmology, 2011
Nasopalpebral lipoma-coloboma syndrome is characterized by nasopalpebral lipoma and eyelid coloboma. We report a case of a 16-year-old Indian girl who reported to us with this rare syndrome.
N Suresh Babu, D Raviprakash, Ravi Kumar
doaj   +1 more source

Excellent outcome of Aspergillous endophthalmitis in a case of allergic bronchopulmonary aspergillosis

open access: yesIndian Journal of Ophthalmology, 2014
While invasive aspergillosis occurs typically in severely immunocompromised patients, cases of surgical site infections have been reported in immunocompetent individuals.
Balbir Khan   +5 more
doaj   +1 more source

Uklanjanje obostranog dermoida na bulbarnoj spojnici šteneta pasmine labrador retriver elektrokauterom - prikaz slučaja. [PDF]

open access: yes, 2013
A Labrador retriever pup with a bilateral dermoid in the eyes was treated successfully by the use of a unipolar hand held electrocautery unit.Štene pasmine labrador retriver s obostranim dermoidom u očima bilo je uspješno izliječeno upotrebom ...
Abhishek C. Saxena   +8 more
core   +1 more source

Repeat gas insufflation for successful closure of idiopathic macular hole following failed primary surgery

open access: yesIndian Journal of Ophthalmology, 2014
A 65-year-old lady presented with decreased vision in left eye since seven months. Vision was 6/9 in right eye and 6/36 in left. Examination revealed idiopathic, full-thickness macular hole in left eye; confirmed by optical coherence tomography (OCT ...
Pukhraj Rishi, Sumanth Reddy, Ekta Rishi
doaj   +1 more source

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