Results 1 to 10 of about 45 (27)

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   +5 more sources

Nasopalpebral Lipoma sine Coloboma Syndrome—First Case Report

open access: yesIndian Journal of Plastic Surgery, 2023
The nasopalpebral lipoma-coloboma syndrome was described for the first time in 1982. It is an autosomal dominant syndrome with complete penetrance and is characterized by features like congenital symmetric upper eyelid and nasopalpebral lipomas ...
Ved Prakash Rao Cheruvu   +3 more
doaj   +3 more sources

Nasopalpebral lipoma‐coloboma syndrome

open access: yesClinical Genetics, 1991
An autosomal dominant dysplasia‐malformation syndrome affecting seven individuals in one family is reported. The components of the syndrome include congenital nasopalpebral lipoma, telecanthus, and bilateral colobomas of upper and lower lids without midface hypoplasia.
A N, Akarsu, B S, Sayli
core   +14 more sources

Diagnosis and treatment of upper eyelid lipoma: A case report. [PDF]

open access: yesAm J Ophthalmol Case Rep, 2020
Purpose: Presentation of a rare lesion: a case of upper eyelid lipoma, Observations: A 76-year-old otherwise healthy woman presented with a right upper eyelid swelling. Her medical history was recorded. On ophthalmologic examination a soft, non-ulcerated
Starnoni M   +3 more
europepmc   +3 more sources

Exome sequencing identifies a de novo frameshift mutation in the imprinted gene ZDBF2 in a sporadic patient with Nasopalpebral Lipoma-coloboma syndrome. [PDF]

open access: yesAm J Med Genet A, 2016
Nasopalpebral lipoma‐coloboma syndrome (NPLCS, OMIM%167730) is an uncommon malformation entity with autosomal dominant inheritance characterized by the combination of nasopalpebral lipoma, colobomas in upper and lower eyelids, telecanthus, and maxillary hypoplasia.
Chacón-Camacho OF   +5 more
europepmc   +4 more sources

Madelung's Disease - Case Series and Treatment by Tumescent Liposuction or Lipectomy. [PDF]

open access: yesOpen Access Maced J Med Sci, 2017
Madelung disease is a disfiguring disorder belonging to the heterogeneous group of lipomatosis. The aetiology is not well understood, but alcohol consumption has been regarded as of importance. The reported incidence is about 1 in 25,000 inhabitants.
Wollina U, Heinig B.
europepmc   +4 more sources

Delayed inflammation associated with retained perfluorocarbon liquid

open access: yesIndian Journal of Ophthalmology, 2011
A 55-year-old woman, with history of cataract surgery 1 year back, presented with features of ocular inflammation for last 3 months. She had no history of any other intraocular surgery.
S Pradeep   +3 more
doaj   +1 more source

Conventional dacryocystorhinostomy in a failed Trans-canalicular laser-assisted dacryocystorhinostomy

open access: yesIndian Journal of Ophthalmology, 2011
We report the success rate and problems associated with conventional dacryocystorhinostomy (DCR) in failed cases of Trans-canalicular, laser-assisted DCR (TCLADCR).
Rajesh Subhash Joshi
doaj   +1 more source

Late occurrence of granular dystrophy in bilateral keratoconus: Penetrating keratoplasty and long-term follow-up

open access: yesIndian Journal of Ophthalmology, 2011
We report a rare case of keratoconus with granular dystrophy with a follow-up of two decades, documenting the sequential presentation of two diseases confirmed by histology and genetic studies.
Varsha M Rathi   +3 more
doaj   +1 more source

Cilioretinal artery occlusion following intranasal cocaine insufflations

open access: yesIndian Journal of Ophthalmology, 2011
Cocaine is used to produce a euphoric effect by abusers, who may be unaware of the devastating systemic and ocular side effects of this drug. We describe the first known case of cilioretinal artery occlusion after intranasal cocaine abuse.
Balaji Kannan   +3 more
doaj   +1 more source

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