HOMEPRODUCTSSERVICESCOMPANYCONTACTFAQResearchDictionaryPharmaMobileSign Up FREE or Login

[A case of congenital non-spherocytic hemolytic anemia caused by triose phosphate isomerase deficiency. Prenatal diagnosis].

Abstract
Prenatal diagnosis: The authors present a personal case of triose-phosphate-isomerase deficiency. Clinically the deficiency associates a constitutional non spherocytic anemia, paroxystic and precocius, and neuromuscular symptoms (axial hypotonia and limb palsies). A diaphragmatic paralysis may complicate the syndrome. Infections are frequent. Survival rarely goes beyond 5 years of age. Biochemical exams show the ubiquity of the deficiency. The physiopathology remains obscure. The TPI deficiency is heritable (autosomal recessive transmission). The gene has been mapped on the short arm of the chromosome 12. Prenatal diagnosis is possible.
AuthorsJ Poinsot, P Parent, D Alix, L Toudic, Y Castel
JournalJournal de génétique humaine (J Genet Hum) Vol. 34 Issue 5 Pg. 431-7 (Nov 1986) ISSN: 0021-7743 [Print] SWITZERLAND
Vernacular TitleUn cas d'anémie hémolytique congénitale non sphérocytaire, par déficit en triose phosphate isomérase. Diagnostic prénatal.
PMID3794669 (Publication Type: Case Reports, English Abstract, Journal Article)
Chemical References
  • Carbohydrate Epimerases
  • Triose-Phosphate Isomerase
Topics
  • Anemia, Hemolytic, Congenital (diagnosis, enzymology, genetics)
  • Carbohydrate Epimerases (deficiency)
  • Female
  • Humans
  • Infant
  • Neuromuscular Diseases (etiology)
  • Pedigree
  • Pregnancy
  • Prenatal Diagnosis
  • Triose-Phosphate Isomerase (deficiency)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research network!


Choose Username:
Email:
Password:
Verify Password: