Käsitteen tiedot
Käytettävä termi
Congenital Hyperinsulinism
Tyyppi
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Topical Descriptor
Alakäsitteet
Ohjaustermit
- Familial Hyperinsulinism
- Familial Hyperinsulinisms
- Hyperinsulinemia Hypoglycemia of Infancy
- Hyperinsulinemic Hypoglycemia, Persistent
- Hyperinsulinemic Hypoglycemias, Persistent
- Hyperinsulinism, Congenital
- Hyperinsulinism, Familial
- Hyperinsulinism, Neonatal
- Hyperinsulinisms, Familial
- Hyperinsulinisms, Neonatal
- Hypoglycemia, Hyperinsulinemic, of Infancy
- Hypoglycemia, Persistent Hyperinsulinemic
- Hypoglycemia, PHHI
- Hypoglycemias, Persistent Hyperinsulinemic
- Hypoglycemias, PHHI
- Infancy Hyperinsulinemia Hypoglycemia
- Infancy Hyperinsulinemia Hypoglycemias
- Neonatal Hyperinsulinism
- Neonatal Hyperinsulinisms
- Persistent Hyperinsulinemia Hypoglycemia of Infancy
- Persistent Hyperinsulinemic Hypoglycemia
- Persistent Hyperinsulinemic Hypoglycemias
- PHHI Hypoglycemia
- PHHI Hypoglycemias
Käyttöhuomautus
- A familial, nontransient HYPOGLYCEMIA with defects in negative feedback of GLUCOSE-regulated INSULIN release. Clinical phenotypes include HYPOGLYCEMIA; HYPERINSULINEMIA; SEIZURES; COMA; and often large BIRTH WEIGHT. Several sub-types exist with the most common, type 1, associated with mutations on an ATP-BINDING CASSETTE TRANSPORTERS (subfamily C, member 8).
Huomautus muutoshistoriasta
- 2014(2004)
Muunkieliset termit
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ruotsi
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suomi
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PPHI-hypoglykemia
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vastasyntyneen pitkittynyt hyperinsulinemiasta johtuva hypoglykemia
URI
http://www.yso.fi/onto/mesh/D044903
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