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Autor:
Kaberi Feroze
Publikováno v:
Kerala Journal of Ophthalmology, Vol 33, Iss 1, Pp 22-28 (2021)
Ocular signs and symptoms have been reported in COVID-19 patients, and there is increasing recognition of conjunctivitis as a prodromal symptom of this disease. There is also a surge of information about corneal, uveal, retinal, and neuroophthalmolog
Autor:
Kalpana Babu, Keerti Mukesh
Publikováno v:
Kerala Journal of Ophthalmology, Vol 33, Iss 1, Pp 3-7 (2021)
We look at the spectrum of uveitis in India before the year 2010 and after the year 2010, the changing patterns in uveitis over time, the probable factors for the changing patterns and newer uveitis entities in India.
Publikováno v:
Medical Journal of Dr. D.Y. Patil Vidyapeeth, Vol 13, Iss 6, Pp 697-699 (2020)
Myasthenia gravis (MG) is a relatively uncommon autoimmune disorder of neuromuscular junction characterized by fatigable muscle weakness, bulbar symptoms, and weakness of extraocular muscles with a significant diurnal variation. Among all other autoi
Publikováno v:
Indian Journal of Pathology and Microbiology, Vol 63, Iss 2, Pp 270-272 (2020)
Basidiobolus ranarum is an uncommon pathogen in ocular infections. It has been previously reported from subcutaneous and gastrointestinal infections. Here, we report a rare case of ocular infection caused by B. ranarum. A 21-year-old male patient pre
Publikováno v:
Indian Journal of Dermatopathology and Diagnostic Dermatology, Vol 6, Iss 2, Pp 100-103 (2019)
Endogenous ochronosis is a manifestation of alkaptonuria, a rare metabolic disease due to homogentisic acid oxidase deficiency. Darkened urine and arthropathy are the other two components that complete the triad of alkaptonuria. Pigmentation of skin,
Publikováno v:
Saudi Journal of Oral Sciences, Vol 6, Iss 1, Pp 41-44 (2019)
Axenfeld–Rieger syndrome (ARS) is a rare, autosomal dominant disorder with genetic and morphologic variability and characterized by ocular and nonocular clinical findings. Midface hypoplasia and maxillary hypodontia are classical presenting feature
Autor:
ErnestNdukaife Anyabolu
Publikováno v:
Sahel Medical Journal, Vol 22, Iss 3, Pp 153-156 (2019)
The incidence of neurofibromatosis (NF), comprising NF-1 and NF-2, seems to be rising in Nigeria. The features of NF-1 have not been completely identified in the country. This case report documents a rare massive lumbar plexiform neurofibroma in NF-1
Autor:
Sunanda Mahajan, Mithali Jage
Publikováno v:
Indian Journal of Dermatopathology and Diagnostic Dermatology, Vol 5, Iss 1, Pp 42-47 (2018)
Introduction: Periorbital hyperpigmentation (POH) is a routinely encountered condition in dermatology practice. Studying the clinical features and its correlation with dermoscopy will help in better understanding of patterns of periorbital pigmentati
Publikováno v:
TNOA Journal of Ophthalmic Science and Research, Vol 57, Iss 2, Pp 155-157 (2019)
Congenital ankyloblepharon describes an eyelid condition when the fused eyelid folds fail to separate and the child is born with completely or partially joined eyelids. Ankyloblepharon is categorized into three types: complete, partial, and interrupt
Publikováno v:
Clinical Dermatology Review, Vol 3, Iss 1, Pp 89-91 (2019)
Lupus vulgaris is a postprimary, chronic form of cutaneous tuberculosis commonly seen over the extremities and gluteal region in Indian population. It is rarely seen over the ears. Lupus vulgaris occurring in the ear was described as “Turkey ear”