Hemophilia

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

Hemophilia was recognized as early as Biblical times when rabbis allowed infant males to be excused from circumcision if two or more of their brothers had previously suffered fatal hemorrhage from the procedure. The specific inheritance pattern of hemophilia was appreciated in 1803, and the disease was given its name by a German physician in 1828. Yet, it was just in 1937 that the disorder was identified as being secondary to deficiency of a plasma globulin rather than to a platelet or vascular abnormality. Our understanding of hemophilia began to advance rapidly in the mid-1960s with the development of plasma concentrates and improved care delivery systems. Whereas a child born with hemophilia 20 to 30 years ago could look forward only to early death or severe crippling, today with proper management such a boy may carry out a nearly normal life style and have even a normal life span.

Original languageEnglish (US)
Pages (from-to)309-326
Number of pages18
JournalPediatric Clinics of North America
Volume27
Issue number2
StatePublished - 1980

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Hemophilia A
Clergy
Inheritance Patterns
Globulins
Names
Blood Vessels
Life Style
Siblings
Blood Platelets
Hemorrhage
Physicians

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

Cite this

Hemophilia. / Buchanan, G. R.

In: Pediatric Clinics of North America, Vol. 27, No. 2, 1980, p. 309-326.

Research output: Contribution to journalArticle

Buchanan, GR 1980, 'Hemophilia', Pediatric Clinics of North America, vol. 27, no. 2, pp. 309-326.
Buchanan, G. R. / Hemophilia. In: Pediatric Clinics of North America. 1980 ; Vol. 27, No. 2. pp. 309-326.
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