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EEC syndrome is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that EEC syndrome, or a subtype of EEC syndrome,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list EEC syndrome as a "rare disease".
Source - Orphanet
Broader types of EEC syndrome:
Complications of EEC syndrome:
see complications of EEC syndrome
Causes of EEC syndrome: see causes of EEC syndrome
Symptoms of EEC syndrome: see symptoms of EEC syndrome
Complications of EEC syndrome: see complications of EEC syndrome
More information:
see contagiousness of EEC syndrome
Inheritance:
see inheritance of EEC syndrome
Misdiagnosis: see misdiagnosis and EEC syndrome.
Doctors and Medical Specialists for EEC syndrome: Medical Geneticist
;
see also doctors and medical specialists for EEC syndrome.
Treatments for EEC syndrome:
see treatments for EEC syndrome
Research for EEC syndrome:
see research for EEC syndrome
Main name of condition: EEC syndrome
Other names or spellings for EEC syndrome:Rudiger syndrome 1, Walker-Clodius Syndrome, cleft lip-cleft palate-lobster claw deformity syndrome, ectrodactyly-cleft lip/palate syndrome, lobster-claw with ectodermal defects syndrome, split hand-cleft lip/palate and ectodermal dysplasia, split hand/feet syndrome, Ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome
Cleft lip-cleft palate-lobster claw deformity syndrome, Ectrodactyly-cleft lip/palate syndrome, Ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome, Rudiger syndrome 1, Walker-Clodius syndrome
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)
Research the causes of these diseases that are similar to, or related to, EEC syndrome:
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