Congenital hemihypertrophy

Known as: Hemihyperplasia, Hemi-hypertrophy, Hemihypertrophy 
A condition in which one side of the body or a part of one side is larger than the other. Children with hemihypertrophy have an increased risk of… (More)
National Institutes of Health

Papers overview

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2014
2014
Somatic mutations in the phosphatidylinositol/AKT/mTOR pathway cause segmental overgrowth disorders. Diagnostic descriptors… (More)
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2004
2004
Sotos syndrome is an overgrowth syndrome characterized by pre- and postnatal overgrowth, macrocephaly, advanced bone age… (More)
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Highly Cited
2003
Highly Cited
2003
Beckwith-Wiedemann syndrome (BWS) is a model imprinting disorder resulting from mutations or epimutations affecting imprinted… (More)
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Review
2001
Review
2001
Neurofibromatosis type 1 (NF1) is the most common of the phakomatoses and has a variety of localized or, more frequently… (More)
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Highly Cited
2000
Highly Cited
2000
Cowden syndrome (CS, MIM 158350) is an autosomal dominant disorder with age related penetrance characterised by multiple… (More)
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Highly Cited
2000
Highly Cited
2000
Germline PTEN mutations cause Cowden syndrome (CS) and Bannayan-Riley-Ruvalcaba syndrome (BRR), two hamartoma-tumour syndromes… (More)
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1999
1999
BACKGROUND Children with Beckwith-Wiedemann syndrome and idiopathic hemihypertrophy (BWS/HH) are at increased risk for developing… (More)
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Highly Cited
1983
Highly Cited
1983
Sir, The increased danger of turnouts developing in children with the exomphalos-macroglossia-gigantism syndrome (Wiedemann… (More)
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