Entry - 278200 - WOOLLY HAIR, HYPOTRICHOSIS, EVERTED LOWER LIP, AND OUTSTANDING EARS - OMIM

 
ICD+
278200

WOOLLY HAIR, HYPOTRICHOSIS, EVERTED LOWER LIP, AND OUTSTANDING EARS


Alternative titles; symbols

SALAMON SYNDROME


Clinical Synopsis
 

Hair
- Woolly hair
- Hypotrichosis
HEENT
- Everted lower lip
- Protruding ears
Inheritance
- ? Autosomal recessive
▲ Close

▼ TEXT

Salamon (1963) described this syndrome as a recessive. The parents were consanguineous. As an isolated trait, woolly hair is a dominant (194300). Also see 278150.


▼ REFERENCES

  1. Salamon, T. Ueber eine Familie mit recessiver Kraushaarigkeit, Hypotrichose und anderen Anomalien. Hautarzt 14: 540-544, 1963. [PubMed: 14113527, related citations]


Creation Date:
Victor A. McKusick : 6/4/1986
Edit History:
mimadm : 3/12/1994
supermim : 3/17/1992
carol : 3/2/1992
supermim : 3/20/1990
ddp : 10/27/1989
marie : 3/25/1988

278200

WOOLLY HAIR, HYPOTRICHOSIS, EVERTED LOWER LIP, AND OUTSTANDING EARS


Alternative titles; symbols

SALAMON SYNDROME


SNOMEDCT: 239023005;   ORPHA: 1409;  



TEXT

Salamon (1963) described this syndrome as a recessive. The parents were consanguineous. As an isolated trait, woolly hair is a dominant (194300). Also see 278150.


REFERENCES

  1. Salamon, T. Ueber eine Familie mit recessiver Kraushaarigkeit, Hypotrichose und anderen Anomalien. Hautarzt 14: 540-544, 1963. [PubMed: 14113527]


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

Edit History:
mimadm : 3/12/1994
supermim : 3/17/1992
carol : 3/2/1992
supermim : 3/20/1990
ddp : 10/27/1989
marie : 3/25/1988



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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