Literature DB >> 3892006

Hyperinsulinaemic hypoglycaemia in an infant with mosaic trisomy 13.

V S Smith, G P Giacoia.   

Abstract

An infant with mosaic trisomy 13, who was small for gestational age, became severely hypoglycaemic. For the first 19 days of life, glucose requirements to maintain normoglycaemia were high (up to 21.7 mg/kg/min) and at the same time the infant had high plasma insulin levels and low glucose insulin ratios. Treatment with hydrocortisone and susphrine was of questionable benefit. Hyperinsulinism abated by the third week of life. This case illustrates early remission of hyperinsulinaemic hypoglycaemia and raises the possibility of an association with trisomy 13.

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Year:  1985        PMID: 3892006      PMCID: PMC1049431          DOI: 10.1136/jmg.22.3.228

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  4 in total

1.  Catecholamine levels in portal, hepatic, and systemic venous blood in portal hypertension.

Authors:  J G Joly; J Leduc; J Bernier; P Lavoie; A Viallet
Journal:  Lancet       Date:  1967-07-15       Impact factor: 79.321

2.  Persistence of hemoglobin F in D/D translocation with trisomy 13-15 (D1).

Authors:  P H Pinkerton; M M Cohen
Journal:  JAMA       Date:  1967-05-15       Impact factor: 56.272

3.  Refractory hypoglycemia associated with a malpositioned umbilical artery catheter.

Authors:  J W Nagel; J S Sims; C E Aplin; E R Westmark
Journal:  Pediatrics       Date:  1979-09       Impact factor: 7.124

4.  Protean manifestations of neonatal hyperinsulinism.

Authors:  T Mayer; M E Matlak; S F Lowry; W M Gooch; D G Johnson
Journal:  Ann Surg       Date:  1981-08       Impact factor: 12.969

  4 in total
  3 in total

Review 1.  Hyperinsulinemic hypoglycemia: clinical, molecular and therapeutical novelties.

Authors:  Arianna Maiorana; Carlo Dionisi-Vici
Journal:  J Inherit Metab Dis       Date:  2017-06-27       Impact factor: 4.982

Review 2.  The Diagnosis and Management of Hyperinsulinaemic Hypoglycaemia.

Authors:  Klára Roženková; Maria Güemes; Pratik Shah; Khalid Hussain
Journal:  J Clin Res Pediatr Endocrinol       Date:  2015-06

3.  Comprehensive screening shows that mutations in the known syndromic genes are rare in infants presenting with hyperinsulinaemic hypoglycaemia.

Authors:  Thomas W Laver; Matthew N Wakeling; Janet Hong Yeow Hua; Jayne A L Houghton; Khalid Hussain; Sian Ellard; Sarah E Flanagan
Journal:  Clin Endocrinol (Oxf)       Date:  2018-09-20       Impact factor: 3.478

  3 in total

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