Hereditary disorders of albumin synthesis

B. A. Buehler

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

Albumin, the major serum protein, is considered to be responsible for maintenance of normal serum colloid osmotic pressure, transport of certain hormones and maintaining an endogenous source of amino acids. The acute loss of albumin in the nephrotic syndrome leads to severe generalized peripheral edema and difficulties in maintenance of normal blood pressure as well as hypocalcemia. Yet, there are now 14 reported cases of congenital analbuminemia in which serum albumin is absent or greatly reduced without clinical evidence of edema, decreased hormone levels or abnormal amino acid requirements. These 'experiments of nature' are reviewed in detail comparing clinical and laboratory findings in these patients with the postulated effects of a low serum albumin level.

Original languageEnglish (US)
Pages (from-to)283-286
Number of pages4
JournalAnnals of Clinical and Laboratory Science
Volume8
Issue number4
StatePublished - Dec 1 1978

Fingerprint

Serum Albumin
Albumins
Edema
Maintenance
Hormones
Amino Acids
Hypocalcemia
Osmotic Pressure
Blood pressure
Nephrotic Syndrome
Colloids
Blood Proteins
Blood Pressure
Serum
Experiments

ASJC Scopus subject areas

  • Microbiology
  • Immunology and Allergy
  • Pathology and Forensic Medicine
  • Immunology
  • Molecular Biology
  • Hematology
  • Clinical Biochemistry
  • Medical Laboratory Technology

Cite this

Hereditary disorders of albumin synthesis. / Buehler, B. A.

In: Annals of Clinical and Laboratory Science, Vol. 8, No. 4, 01.12.1978, p. 283-286.

Research output: Contribution to journalArticle

Buehler, B. A. / Hereditary disorders of albumin synthesis. In: Annals of Clinical and Laboratory Science. 1978 ; Vol. 8, No. 4. pp. 283-286.
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