WebCogan syndrome is a rare autoimmune disease involving the eye and the inner ear. Cogan syndrome affects young adults, with 80% of patients between 14 and 47 years. The disease appears to result from an autoimmune reaction directed against an unknown common autoantigen in the cornea and inner ear. About 10 to 30% of patients also have severe ... WebCase Report. A 28-yr-old woman with Cohen syndrome was scheduled to undergo magnetic resonance imaging (MRI) of her right knee.The patient had been diagnosed with Cohen syndrome as an infant because of mental retardation, micrognathia, prominent upper central incisors, and obesity ().The patient had moderate mental retardation and …
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WebOct 1, 2024 · An autosomal recessive disorder characterized by retinitis pigmentosa; polydactyly; obesity; mental retardation; hypogenitalism; renal dysplasia; and short … WebPrimary aldosteronism (PA), also known as primary hyperaldosteronism or Conn's syndrome, refers to the excess production of the hormone aldosterone from the adrenal glands, resulting in low renin levels and high blood pressure. This abnormality is caused by hyperplasia or tumors.Many experience fatigue, potassium deficiency and high blood … psa 56 anni
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WebCogan’s syndrome (also Cogan syndrome) is an uncommon disease seen mostly in young adults that can severely affect vision and hearing. [1][2]This syndrome was described by … WebJan 22, 2024 · From OMIM Cohen-Gibson syndrome (COGIS) is an overgrowth disorder characterized by increased somatic parameters apparent from birth and associated with variable intellectual disability. Affected individuals have dysmorphic facial features, advanced bone age, and skeletal abnormalities, including flaring of the metaphyses of … WebCohen syndrome is an inherited disorder that affects many parts of the body and is characterized by developmental delay, intellectual disability, small head size ( microcephaly ), and weak muscle tone (hypotonia). psa 6 blastoise