LADD Syndrome


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Important

It is possible that the main title of the report LADD Syndrome is not the name you expected. Please check the synonyms listing to find the alternate name(s) and disorder subdivision(s) covered by this report.


Synonyms


  • Lacrimo-Auriculo-Dento-Digital Syndrome
  • LADD
  • Levy-Hollister Syndrome
  • Limb Malformations-Dento-Digital Syndrome

Disorder Subdivisions


  • None

General Discussion


LADD Syndrome is a rare genetic disorder characterized primarily by malformations of the upper limbs and inherited through an autosomal dominant trait. Other symptoms of the disorder may include: malformations in the structures and ducts that secrete tears and drain them from the surface of the eyeball (the lacrimal apparatus); abnormalities of the teeth; small cupped ears; absent or underdeveloped salivary glands; hearing loss; abnormalities of the sexual and urinary system of the body (genitourinary) and/or unusual skin ridge patterns.


Resources


NIH/National Arthritis and Musculoskeletal and Skin Diseases Information Clearinghouse

1 AMS Circle

Bethesda, MD 20892-3675

USA

Tel: 3014954484

Fax: 3017186366

Tel: 8772264267

TDD: 3015652966

Email: NIAMSinfo@mail.nih.gov

Internet: http://www.niams.nih.gov



Genetic and Rare Diseases (GARD) Information Center

PO Box 8126

Gaithersburg, MD 20898-8126

Tel: (301)519-3194

Fax: (240)632-9164

Tel: (888)205-2311

TDD: (888)205-3223

Email: gardinfo@nih.gov

Internet: http://www.genome.gov/100000409 or http://rarediseases.info.nih.gov/html/resources/info_cntr.html




For a Complete Report


This is an abstract of a report from the National Organization for Rare Disorders, Inc. ® (NORD). A copy of the complete report can be obtained for a small fee by visiting the NORD website. The complete report contains additional information including symptoms, causes, affected population, related disorders, standard and investigational treatments (if available), and references from medical literature. For a full-text version of this topic, see http://www.rarediseases.org/search/rdblist.html

The information provided in this report is not intended for diagnostic purposes. It is provided for informational purposes only. NORD recommends that affected individuals seek the advice or counsel of their own personal physicians.

It is possible that the title of this topic is not the name you selected. Please check the Synonyms listing to find the alternate name(s) and Disorder Subdivision(s) covered by this report.

This disease entry is based upon medical information available through the date at the end of the topic. Since NORD's resources are limited, it is not possible to keep every entry in the Rare Disease Database completely current and accurate. Please check with the agencies listed in the Resources section for the most current information about this disorder.

For additional information and assistance about rare disorders, please contact the National Organization for Rare Disorders at P.O. Box 1968, Danbury, CT 06813-1968; phone (203) 744-0100; web site www.rarediseases.org or email orphan@rarediseases.org

Last Updated:   8/7/2007

Copyright   1992, 1999, 2007 National Organization for Rare Disorders, Inc.


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Last updated: August 07, 2007

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