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Otitis externa. A moderate case of otitis externa. There is narrowing of the ear channel, with a small amount of exudate and swelling of the outer ear. Otitis externa, also called swimmer's ear, [1] is inflammation of the ear canal. [2] It often presents with ear pain, swelling of the ear canal, and occasionally decreased hearing. [2]
Perichondritis is inflammation of the perichondrium, a layer of connective tissue which surrounds cartilage. [2] A common form, auricular perichondritis ( perichondritis auriculae ) involves infection of the pinna due to infection of traumatic or surgical wound or the spread of inflammation into depth (e.g. Infected transcartilaginous ear ...
Parinaud's syndrome is a constellation of neurological signs indicating injury to the dorsal midbrain. More specifically, compression of the vertical gaze center at the rostral interstitial nucleus of medial longitudinal fasciculus (riMLF). It is a group of abnormalities of eye movement and pupil dysfunction and is named for Henri Parinaud [6 ...
The most common cause of POS is cat-scratch disease, an infectious disease that typically results from a scratch or bite from a cat. However, this syndrome is an unusual feature of cat-scratch disease. In rare cases, other infections may also cause the syndrome. [1] Bartonella henselae [2] Francisella tularensis [3] Herpes simplex virus type 1 [4]
Alport syndrome. Alport syndrome is a genetic disorder [ 1 ] affecting around 1 in 5,000–10,000 children, [ 2 ] characterized by glomerulonephritis, end-stage kidney disease, and hearing loss. [ 3 ] Alport syndrome can also affect the eyes, though the changes do not usually affect vision, except when changes to the lens occur in later life.
Ear pain. Other names. Otalgia, earache. Examination of the ear canal and eardrum. Specialty. ENT surgery. Ear pain, also known as earache or otalgia, is pain in the ear. [1][2] Primary ear pain is pain that originates from the ear. Secondary ear pain is a type of referred pain, meaning that the source of the pain differs from the location ...
Leber congenital amaurosis. Leber congenital amaurosis (LCA) is a rare inherited eye disease that appears at birth or in the first few months of life. [2] It affects about 1 in 40,000 newborns. [1] LCA was first described by Theodor Leber in the 19th century. [3][4] It should not be confused with Leber's hereditary optic neuropathy, which is a ...
Rheumatology. Saethre–Chotzen syndrome (SCS), also known as acrocephalosyndactyly type III, is a rare congenital disorder associated with craniosynostosis (premature closure of one or more of the sutures between the bones of the skull). This affects the shape of the head and face, resulting in a cone-shaped head and an asymmetrical face.