Fryns syndrome

Fryns syndrome is a condition that affects the development of many parts of the body. The features of this disorder vary widely among affected individuals and overlap with the signs and symptoms of several other disorders. These factors can make ...1

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Symptoms of Fryns syndrome

Symptoms: The Human Phenotype Ontology (HPO) provides the following list of features that have been reported in people with this condition. Much of the information in the HPO comes from Orphanet, a European rare disease database. Signs and Symptoms

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Causes of Fryns syndrome

Cause: Although the exact cause of Fryns syndrome is unknown, it is thought to be genetic because it tends to "run in families" and has features common to other genetic disorders.[1, 2][3] Several chromosomal abnormalities involving chromosome bands ...2

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Genetics of Fryns syndrome

Genetic Changes: The cause of Fryns syndrome is unknown. The disorder is thought to be genetic because it tends to run in families and has features similar to those of other genetic disorders. Duplications and deletions in several chromosome regions ...3

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Names and Terminology

Other Names for This Condition

Source: GHR (NLM/NIH)4 ...

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  1. Source: GHR (NLM/NIH): condition/ fryns-syndrome
  2. Source: GARD (NIH): diseases/ 3699/ fryns-syndrome
  3. Source: GHR (NLM/NIH): condition/ fryns-syndrome
  4. ibid.

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