 Congenital Hyperinsulinism
"Congenital Hyperinsulinism" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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).
| Descriptor ID |
D044903
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| MeSH Number(s) |
C06.689.150 C16.614.200 C18.452.394.968.250 C18.452.394.984.200
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| Concept/Terms |
Congenital Hyperinsulinism- Congenital Hyperinsulinism
- Congenital Hyperinsulinisms
- Hyperinsulinisms, Congenital
- Hyperinsulinemia Hypoglycemia of Infancy
- Infancy Hyperinsulinemia Hypoglycemias
- Hyperinsulinemic Hypoglycemia, Persistent
- Hyperinsulinemic Hypoglycemias, Persistent
- Hypoglycemia, Persistent Hyperinsulinemic
- Hypoglycemias, Persistent Hyperinsulinemic
- Persistent Hyperinsulinemic Hypoglycemias
- Hyperinsulinism, Congenital
- Hyperinsulinism, Familial
- Familial Hyperinsulinisms
- Hyperinsulinisms, Familial
- PHHI Hypoglycemia
- Hypoglycemia, PHHI
- Hypoglycemias, PHHI
- PHHI Hypoglycemias
- Hypoglycemia, Hyperinsulinemic, of Infancy
- Infancy Hyperinsulinemia Hypoglycemia
- Neonatal Hyperinsulinism
- Persistent Hyperinsulinemia Hypoglycemia of Infancy
- Persistent Hyperinsulinemic Hypoglycemia
- Familial Hyperinsulinism
- Hyperinsulinism, Neonatal
- Hyperinsulinisms, Neonatal
- Neonatal Hyperinsulinisms
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Below are MeSH descriptors whose meaning is more general than "Congenital Hyperinsulinism".
Below are MeSH descriptors whose meaning is more specific than "Congenital Hyperinsulinism".
This graph shows the total number of publications written about "Congenital Hyperinsulinism" by people in this website by year, and whether "Congenital Hyperinsulinism" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2004 | 0 | 1 | 1 | | 2017 | 1 | 0 | 1 |
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Below are the most recent publications written about "Congenital Hyperinsulinism" by people in Profiles.
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Cabezas OR, Flanagan SE, Stanescu H, García-Martínez E, Caswell R, Lango-Allen H, Antón-Gamero M, Argente J, Bussell AM, Brandli A, Cheshire C, Crowne E, Dumitriu S, Drynda R, Hamilton-Shield JP, Hayes W, Hofherr A, Iancu D, Issler N, Jefferies C, Jones P, Johnson M, Kesselheim A, Klootwijk E, Koettgen M, Lewis W, Martos JM, Mozere M, Norman J, Patel V, Parrish A, Pérez-Cerdá C, Pozo J, Rahman SA, Sebire N, Tekman M, Turnpenny PD, Hoff WV, Viering DHHM, Weedon MN, Wilson P, Guay-Woodford L, Kleta R, Hussain K, Ellard S, Bockenhauer D. Polycystic Kidney Disease with Hyperinsulinemic Hypoglycemia Caused by a Promoter Mutation in Phosphomannomutase 2. J Am Soc Nephrol. 2017 08; 28(8):2529-2539.
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Magge SN, Shyng SL, MacMullen C, Steinkrauss L, Ganguly A, Katz LE, Stanley CA. Familial leucine-sensitive hypoglycemia of infancy due to a dominant mutation of the beta-cell sulfonylurea receptor. J Clin Endocrinol Metab. 2004 Sep; 89(9):4450-6.
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