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Achromatopsia. Achromatopsia, also known as rod monochromacy, is a medical syndrome that exhibits symptoms relating to five conditions, most notably monochromacy. Historically, the name referred to monochromacy in general, but now typically refers only to an autosomal recessive congenital color vision condition.
Males are more likely to inherit red–green color blindness than females, because the genes for the relevant opsins are on the X chromosome. [1] Screening for congenital red–green color blindness is typically performed with the Ishihara or similar color vision test. [1] There is no cure for color blindness. [1]
Color blindness or color vision deficiency ( CVD) is the decreased ability to see color or differences in color. [ 2] The severity of color blindness ranges from mostly unnoticeable to full absence of color perception. Color blindness is usually an inherited problem or variation in the functionality of one or more of the three classes of cone ...
Psychosis, delirium, or dementia [ 1] Visual release hallucinations, also known as Charles Bonnet syndrome or CBS, are a type of psychophysical visual disturbance in which a person with partial or severe blindness experiences visual hallucinations . First described by Charles Bonnet in 1760, [ 2][ 3] the term Charles Bonnet syndrome was first ...
An occurrence of central serous retinopathy of the fovea centralis imaged using optical coherence tomography. Specialty. Ophthalmology. Central serous chorioretinopathy ( CSC or CSCR ), also known as central serous retinopathy ( CSR ), is an eye disease that causes visual impairment, often temporary, usually in one eye. [ 1][ 2] When the ...
Incontinentia pigmenti. This condition is inherited in an X-linked dominant manner. Incontinentia pigmenti ( IP) is a rare X-linked dominant genetic disorder that affects the skin, hair, teeth, nails and central nervous system. It is named from its appearance under a microscope. [ 1]
Heterochromia iridum. Heterochromia is a variation in coloration most often used to describe color differences of the iris, but can also be applied to color variation of hair [ 1] or skin. Heterochromia is determined by the production, delivery, and concentration of melanin (a pigment ). It may be inherited, or caused by genetic mosaicism ...
ICD-10 is the 10th revision of the International Classification of Diseases (ICD), a medical classification list by the World Health Organization (WHO). It contains codes for diseases, signs and symptoms, abnormal findings, complaints, social circumstances, and external causes of injury or diseases. [ 1] Work on ICD-10 began in 1983, [ 2 ...