Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0042961 (volvulus)
 4,305 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Abomasal hypomotility is a prerequisite for abomasal displacement in cattle and is present immediately after surgical correction of left displaced abomasum or abomasal volvulus. Hypocalcemia, hypokalemia, and hyperinsulinemia should be corrected in cattle suspected to have abomasal hypomotility. The most effective prokinetic for calves and adult cattle suspected to have abomasal hypomotility is erythromycin.
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PMID:Evidence-based use of prokinetic drugs for abomasal disorders in cattle. 2237 17

Congenital hyperinsulinism (CHI) is a rare glucose metabolism disorder characterized by unregulated secretion of insulin leading to hyperinsulinemic hypoglycemia (HH). Most cases are caused by mutations in the KATP-channel genes ABCC8 and KCNJ11. We report two patients with severe HH from the first day of life. Patient 1 developed midgut volvulus after initiating diazoxide and required intestinal resection. He was subsequently managed with high-dose octreotide and glucose enriched diet. Consistent with diffuse type CHI by 18F-DOPA-PET/CT, genetic testing revealed a homozygous ABCC8 variant, c.1801G>A, p.(Val601Ile). The rare variant was previously reported to be diazoxide-responsive and the patient responded well to diazoxide monotherapy with clinical remission at two years of age. Patient 2 responded to diazoxide with spontaneous clinical remission at 15 months of age. However, an oral glucose tolerance test at seven years of age revealed hyperinsulinism. Genetic testing revealed the proband and several seemingly healthy family members harbored a novel, heterozygous ABCC8 variant, c.1780T>C, p.(Ser594Pro). Genetic findings identified previously unrecognized HH in the proband.
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PMID:Congenital Hyperinsulinism: Two case reports with different rare variants in ABCC8. 3287 44