Entry - 136200 - FLUSHING OF EARS AND SOMNOLENCE - OMIM

 
 
136200

FLUSHING OF EARS AND SOMNOLENCE


Clinical Synopsis
 

Skin
- Intermittent episodes of ear flushing
Neuro
- Somnolence
Inheritance
- Autosomal dominant
▲ Close

▼ TEXT

Kim (1969) noted a father and 2 sons, aged 7 and 11 years, with intermittent episodes of flushing of the ears associated with somnolence. It had its onset in all 3 at about the same time. The mother and another son were unaffected.

▼ REFERENCES

  1. Kim, P. M. Familial flushing and somnolence. (Letter) JAMA 210: 1289 only, 1969.


Creation Date:
Victor A. McKusick : 6/4/1986
Edit History:
terry : 06/03/2009
mimadm : 9/24/1994
supermim : 3/16/1992
supermim : 3/20/1990
ddp : 10/26/1989
marie : 3/25/1988
reenie : 6/4/1986

136200

FLUSHING OF EARS AND SOMNOLENCE



TEXT

Kim (1969) noted a father and 2 sons, aged 7 and 11 years, with intermittent episodes of flushing of the ears associated with somnolence. It had its onset in all 3 at about the same time. The mother and another son were unaffected.

REFERENCES

  1. Kim, P. M. Familial flushing and somnolence. (Letter) JAMA 210: 1289 only, 1969.


Creation Date:
Victor A. McKusick : 6/4/1986

Edit History:
terry : 06/03/2009
mimadm : 9/24/1994
supermim : 3/16/1992
supermim : 3/20/1990
ddp : 10/26/1989
marie : 3/25/1988
reenie : 6/4/1986



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 8, 2024