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A Mysterious Central Scotoma in a Teenage Male Patient.

07:00 EST 13th February 2020 | BioPortfolio

Summary of "A Mysterious Central Scotoma in a Teenage Male Patient."

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This article was published in the following journal.

Name: JAMA ophthalmology
ISSN: 2168-6173
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Medical and Biotech [MESH] Definitions

A maternally linked genetic disorder that presents in mid-life as acute or subacute central vision loss leading to central scotoma and blindness. The disease has been associated with missense mutations in the mtDNA, in genes for Complex I, III, and IV polypeptides, that can act autonomously or in association with each other to cause the disease. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/Omim/, MIM#535000 (April 17, 2001))

MYCOBACTERIUM infections of the male reproductive tract (GENITALIA, MALE).

Pathological processes involving the male reproductive tract (GENITALIA, MALE).

Pathological processes of the male URINARY TRACT and the reproductive system (GENITALIA, MALE).

The inability of the male to effect FERTILIZATION of an OVUM after a specified period of unprotected intercourse. Male sterility is permanent infertility.

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