Overgrowth syndrome · Group of rare genetic disorders involving tissue hypertrophy · YYNN

Overgrowth syndrome

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Group of rare genetic disorders involving tissue hypertrophy

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Instances
1

Tatton-Brown–Rahman syndrome

Overgrowth syndrome caused by DNMT3A gene mutation

Subclasses
2

Fragile X syndrome

X-linked dominant genetic disorder

Weaver syndrome

Rare genetic overgrowth disorder

Subject of
1

Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disability.

scientific article published on 09 March 2014

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Overgrowth syndromes in children constitute a group of rare disorders that are characterised by tissue hypertrophy. Individual overgrowth syndromes have been shown to overlap with regard to clinical and radiologic features. The details of the genetic bases of these syndromes are unfolding. Any of the three embryonic tissue layers may be...

Instance of

developmental defect during embryogenesis

Genetic disorder

class of disease

Subclass of

Malformative syndrome

rare genetic developmental defect during embryogenesis

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