Entry - 145200 - HYPERPIGMENTATION OF FULDAUER AND KUIJPERS - OMIM

 
 
145200

HYPERPIGMENTATION OF FULDAUER AND KUIJPERS


Clinical Synopsis
 

Skin
- Hyperpigmentation of wrists, hands, neck and less consistently on axillary folds, dorsa of the feet and lines of hands
Inheritance
- Autosomal dominant
▲ Close

▼ TEXT

Fuldauer and Kuijpers (1964) described a pigmentary anomaly in many members of a Dutch family. Although the paper was entitled 'Incontinentia Pigmenti,' the distribution of the hyperpigmentation was quite different, being located on the wrists, hands, and neck and less consistently on the axillary folds, dorsa of the feet, and lines of the hands. Furthermore, incontinentia pigmenti is probably an X-linked dominant lethal in males. Many males were affected in this family.


▼ REFERENCES

  1. Fuldauer, M. L., Kuijpers, P. B. An inherited pigmentary anomaly (incontinentia pigmenti)? Nederl. T. Geneesk. 108: 1613-1623, 1964. [PubMed: 14222004, related citations]


Creation Date:
Victor A. McKusick : 6/2/1986
Edit History:
terry : 04/30/1999
mimadm : 9/24/1994
supermim : 3/16/1992
supermim : 3/20/1990
ddp : 10/27/1989
marie : 3/25/1988
reenie : 6/2/1986

145200

HYPERPIGMENTATION OF FULDAUER AND KUIJPERS



TEXT

Fuldauer and Kuijpers (1964) described a pigmentary anomaly in many members of a Dutch family. Although the paper was entitled 'Incontinentia Pigmenti,' the distribution of the hyperpigmentation was quite different, being located on the wrists, hands, and neck and less consistently on the axillary folds, dorsa of the feet, and lines of the hands. Furthermore, incontinentia pigmenti is probably an X-linked dominant lethal in males. Many males were affected in this family.


REFERENCES

  1. Fuldauer, M. L., Kuijpers, P. B. An inherited pigmentary anomaly (incontinentia pigmenti)? Nederl. T. Geneesk. 108: 1613-1623, 1964. [PubMed: 14222004]


Creation Date:
Victor A. McKusick : 6/2/1986

Edit History:
terry : 04/30/1999
mimadm : 9/24/1994
supermim : 3/16/1992
supermim : 3/20/1990
ddp : 10/27/1989
marie : 3/25/1988
reenie : 6/2/1986



NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2024 Johns Hopkins University.

NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.
OMIM® and Online Mendelian Inheritance in Man® are registered trademarks of the Johns Hopkins University.
Copyright® 1966-2024 Johns Hopkins University.
Printed: June 9, 2024