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Что (кто) такое Kocher"s syndrome - определение

MUSCULAR PSEUDOHYPERTROPHY - HYPOTHYROIDISM, ALSO KNOWN AS KOCHER-DEBRE-SEMELAIGNE SYNDROME IS A RARE DISORDER CHARACTERIZED BY PSEUDOHYPERTROPHY OF MUSCLES DUE TO LONGSTANDING HYPOTHYROIDISM (SEE THIS TERM)

Kocher-Debré-Semélaigne syndrome; Kocher-Debre-Semelaigne syndrome

Kocher–Debre–Semelaigne syndrome

Kocher–Debré–Semelaigne syndrome is hypothyroidism in infancy or childhood characterised by lower extremity or generalized muscular hypertrophy, myxoedema, short stature and cognitive impairment. The absence of painful spasms and pseudomyotonia differentiates this syndrome from its adult form, which is Hoffmann syndrome.

https://en.wikipedia.org/wiki/Kocher–Debre–Semelaigne_syndrome

Reye's syndrome

SYNDROME CHARACTERIZED BY ACUTE BRAIN DAMAGE AND LIVER FUNCTION PROBLEMS

Reyes Syndrome; Reye Syndrome; Reye's Syndrome; Reyes syndrome; Reye’s Syndrome; Reye hepatocerebral syndrome; Rye syndrome; Reye s syndrome; Reye's s syndrome; Reye's syndrome; Reye’s syndrome

['re?z, 'r??z]

¦ noun a life-threatening metabolic disorder in young children, of uncertain cause.

Origin

1960s: named after the Australian paediatrician Ralph D. K. Reye.

Stewart–Treves syndrome

HUMAN DISEASE

Stewart-treves syndrome; Stewart–Treves Syndrome; Postmastectomy lymphangiosarcoma; Stewart Treves syndrome; Cutaneous angiosarcoma; Stewart-Treves syndrome; Stewart-Treves Syndrome

Stewart–Treves syndrome refers to a lymphangiosarcoma, a rare disorder marked by the presence of an angiosarcoma (a malignant tumor of blood or lymph vessels) in a person with chronic (long-term) lymphedema. Although it most commonly refers to malignancies associated with chronic lymphedema resulting from mastectomy and/or radiotherapy for breast cancer, it may also describe lymphangiosarcomas that result from congenital and other causes of chronic secondary lymphedema.

https://en.wikipedia.org/wiki/Stewart–Treves_syndrome

Википедия

Kocher–Debre–Semelaigne syndrome

Kocher–Debré–Semelaigne syndrome is hypothyroidism in infancy or childhood characterised by lower extremity or generalized muscular hypertrophy, myxoedema, short stature and cognitive impairment. The absence of painful spasms and pseudomyotonia differentiates this syndrome from its adult form, which is Hoffmann syndrome.

The syndrome is named after Emil Theodor Kocher, Robert Debré and Georges Semelaigne. Also known as Debré–Semelaigne syndrome or cretinism-muscular hypertrophy, hypothyroid myopathy, hypothyroidism-large muscle syndrome, hypothyreotic muscular hypertrophy in children, infantile myxoedema-muscular hypertrophy, myopathy-myxoedema syndrome, myxoedema-muscular hypertrophy syndrome, myxoedema-myotonic dystrophy syndrome.

Kocher–Debre–Semelaigne syndrome gives the infant a Hercules appearance.

https://en.wikipedia.org/wiki/Kocher–Debre–Semelaigne syndrome