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How is CdLS recognized?

Last modified by Gerritjan Koekkoek on 2011/05/14 11:00

CdLS is a congenital syndrome, meaning it is present from birth. Most of the signs and symptoms may be recognized at birth or shortly thereafter. A child need not demonstrate each and every sign or symptom for the diagnosis to be made.

As with other syndromes, individuals with CdLS strongly resemble one another. Common characteristics include: low birthweight (often under five pounds), slow growth and small stature, and small head size (microcephaly). Typical facial features include thin eyebrows which frequently meet at midline (synophrys), long eyelashes, short upturned nose and thin, downturned lips.

Other frequent findings include excessive body hair (hirsutism), small hands and feet, partial joining of the second and third toes, incurved fifth fingers, gastroesophageal reflux, seizures, heart defects, cleft palate, bowel abnormalities, feeding difficulties, and developmental delay. Limb differences, including missing limbs or portions of limbs, usually fingers, hands or forearms, are also found in some individuals.

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Created by Gerritjan Koekkoek on 2009/06/25 20:15

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World associations

CdLS is worldwide present, all information is available in English
but if you want to change the language click on a flag of one of the supportgroups in CdLS World
Number of associations: 19
Australia
Australia
Australia
Canada
Deutschland
España
France
Italia
vereniging CdLS
vereniging CdLS
Polska
Portugal
CdLS Foundation UK & Ireland
CdLS Foundation UK & Ireland
CdLS Foundation USA
Danmark
日本
Schweiz, Suisse
CdLS World
Chile
South Korea
Central America
Central America
Central America
Central America
Central America
Argentina

Disclaimer - All of the information contained within these questions and answers is for education purposes only. The place to get specific medical advice, diagnoses, and treatment is your doctor. Use of this site is strictly at your own risk. If you find something that you think needs correction or clarification, please let us know at: umugler@aol.com
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