Results 51 to 60 of about 1,679 (131)

High‐Power Surgical Laser for Treatment of Oral Manifestations of Mucopolysaccharidosis VI: A Case Report

open access: yesSpecial Care in Dentistry, Volume 46, Issue 4, July/August 2026.
ABSTRACT Mucopolysaccharidosis type VI (MPS VI), a rare metabolic disorder, results from glycosaminoglycan accumulation in tissues, frequently leading to hyperplastic gingival alterations that necessitate comprehensive intervention. An 11‐year‐old male patient diagnosed with MPS VI required hospitalization due to complications associated with a ...
Regina Maria Raffaele   +5 more
wiley   +1 more source

Caroticocavernous Fistulae: Clinical Presentation, Imaging, and Endovascular Treatment

open access: yesJournal of Clinical Interventional Radiology ISVIR, 2019
Caroticocavernous fistulas (CCFs) occur due to an abnormal communication between the high-pressure carotid artery system and the relatively lower pressure cavernous sinus system.
Pushpinder S. Khera   +8 more
doaj   +1 more source

Malignant melanoma of the rectum presenting as orbital metastasis

open access: yesIndian Journal of Ophthalmology, 2020
An orbital mass being the presenting sign of disseminated systemic metastasis is a rare clinical picture. Here, the authors describe the case of a 52-year old Asian-Indian female who presented with unilateral proptosis and motility restriction.
Natasha Narayanan   +4 more
doaj   +1 more source

Idiopathic Orbital Inflammation Masquerading as Relapse of Seronegative Juvenile Myasthenia Gravis: A Case Report

open access: yes
Journal of Paediatrics and Child Health, EarlyView.
Wenhao Duan   +4 more
wiley   +1 more source

Expanding the Phenotypic Spectrum of Degcags Syndrome: Novel Craniofacial and Oral Findings

open access: yesSpecial Care in Dentistry, Volume 46, Issue 4, July/August 2026.
ABSTRACT Aims: Developmental delay with gastrointestinal, cardiovascular, genitourinary, and skeletal abnormalities (DEGCAGS) syndrome (OMIM #619488) is a rare autosomal recessive disorder caused by pathogenic variants in ZNF699 and characterized by developmental delay and multisystem involvement.
Jeferson Paiva   +8 more
wiley   +1 more source

Schwannoma- A Rare Cause of Proptosis

open access: yesJournal of the Dow University of Health Sciences, 2022
Schwannoma  a tumor of cranial and peripheral nerves is rarely found in the orbit and if present causes proptosis. We report a rare cause of unilateral proptosis .
Maeirah Shafique   +4 more
doaj  

Unusual Presentation of Orbital Neuroblastoma after Evisceration

open access: yesDelhi Journal of Ophthalmology, 2012
This is a case report of a 17 year old girl having protruding mass from evicerated left eye which was associated with severe ocular pain. Mass was about 3.6 × 5.8 cm in size, histopathological examination and immunohistochemistry report confirm ...
Swati Kujur, Devesh Khandey
doaj   +1 more source

Maxillofacial Cemento‐Ossifying Fibroma: A Rare Case Report

open access: yesClinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Cemento‐ossifying fibroma is a relatively rare lesion affecting the jaws, especially the anterior mandible. The most common clinical presentation is swelling. Diagnosis based on clinical observation only is challenging. Radiological images and histological findings can be misleading due to similitudes with other osteo‐fibrous lesions.
Alix N. Kamina   +5 more
wiley   +1 more source

Clinical profiles of thyroid eye disease with and without strabismus: a comparative study [PDF]

open access: yesInternational Journal of Ophthalmology
AIM: To identify differences in clinical features between thyroid eye disease (TED) patients with and without strabismus. METHODS: This retrospective, single-center, consecutive case series study was conducted on TED patients who were determined to be ...
Masoud Khorrami-Nejad   +6 more
doaj   +1 more source

10.4274/tjo.42.00821

open access: yesTürk Oftalmoloji Dergisi, 2012
Slowly progressing unilateral proptosis occurred in a male patient with a history of trauma experienced 2 years ago. All the ophthalmological examination, laboratory investigation, and both neurological and hematological evaluations were normal and ...
Esin Tunca Kırıkkaya   +3 more
doaj   +1 more source

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