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PMID: 1999344 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Incidence of Menkes disease.

Human genetics ·Vol. 86 ·No. 4 ·1991-02-00 ·Pages 408-10

Tønnesen T, Kleijer WJ, Horn N

Abstract

We have calculated the incidence of Menkes disease for Denmark, France, The Netherlands, the United Kingdom and West Germany, based on known Menkes patients born during the time period 1976-87. Considering live-born Menkes patients, the combined incidence for these five countries is 1 Menkes patient per 298,000 live-born babies. If the number of affected aborted fetuses are taken into account, the incidence is 1 Menkes per 254,000 live-born babies. This incidence, which is 2-4 times lower than earlier published incidence figures, places Menkes disease as an extremely rare disease. The mutation rate for Menkes disease is estimated to be 1.96 x 10(-6), based on the number of isolated Menkes cases born during the time period 1976-87 and the total number of newborn males during this time.

MeSH Terms
Denmark France Germany, West Humans Incidence Infant, Newborn Menkes Kinky Hair Syndrome/epidemiology,genetics Netherlands United Kingdom X Chromosome
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Tønnesen T
John F. Kennedy Institute, Glostrup, Denmark.
Kleijer W J
Horn N
References (5)
5 references, click to expand
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    Ergeb Inn Med Kinderheilkd. 1988;57:77-144 PMID: 3063527
  2. First-trimester diagnosis of Menkes disease: intermediate copper values in chorionic villi from three affected male fetuses.
    Prenat Diagn. 1989 Mar;9(3):159-65 PMID: 2710742
  3. Copper incorporation studies on cultured cells for prenatal diagnosis of Menkes' disease.
    Lancet. 1976 May 29;1(7970):1156-8 PMID: 58201
  4. Menkes's kinky hair syndrome. An inherited defect in copper absorption with widespread effects.
    Pediatrics. 1972 Aug;50(2):188-201 PMID: 5045349
  5. A sex-linked recessive disorder with retardation of growth, peculiar hair, and focal cerebral and cerebellar degeneration.
    Pediatrics. 1962 May;29:764-79 PMID: 14472668
Article Info
Journal
Human genetics
Abbr.
Hum Genet
ISSN
0340-6717
Published
1991-02-00
Pages
408-10
Language
English
Region
Germany
NLM ID
7613873
Subset
IM
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