(Q36554428)

14 August 2017

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title

The challenges of Proteus syndrome: diagnosis and management (English)

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14 August 2017

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1

Leslie Biesecker

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14 August 2017

2 August 2006

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European Journal of Human Genetics

14 August 2017

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14 August 2017

14

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14 August 2017

11

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14 August 2017

1151-1157

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https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201638

14 August 2017

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cites work

The proteus syndrome. Partial gigantism of the hands and/or feet, nevi, hemihypertrophy, subcutaneous tumors, macrocephaly or other skull anomalies and possible accelerated growth and visceral affections

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201638

Proteus syndrome: diagnostic criteria, differential diagnosis, and patient evaluation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201638

Clinical differentiation between Proteus syndrome and hemihyperplasia: description of a distinct form of hemihyperplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201638

Reassessment of the Proteus syndrome literature: application of diagnostic criteria to published cases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201638

Evolution of skin lesions in Proteus syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201638

Encephalocraniocutaneous lipomatosis and Proteus syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201638

Germline mutation of the tumour suppressor PTEN in Proteus syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201638

Germline and germline mosaic PTEN mutations associated with a Proteus-like syndrome of hemihypertrophy, lower limb asymmetry, arteriovenous malformations and lipomatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201638

Screening for Wilms' tumor in children with high-risk congenital syndromes: considerations for an intervention trial

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201638

Proteus syndrome: an update

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201638

Proteus syndrome: Misdiagnosis with PTEN mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201638

PTEN mutations are uncommon in Proteus syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201638

Considerations for a multiaxis nomenclature system for medical genetics.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201638

Neoplasms in Proteus syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201638

Lethal genes surviving by mosaicism: a possible explanation for sporadic birth defects involving the skin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201638

Association of germline mutation in the PTEN tumour suppressor gene and Proteus and Proteus-like syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201638

The multifaceted challenges of Proteus syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201638

7 January 2021

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201638

1 reference

7 January 2021

PTEN mutations and proteus syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201638

7 January 2021

Causes of premature death in Proteus syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201638

7 January 2021

Sudden death caused by pulmonary thromboembolism in Proteus syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201638

7 January 2021

Cutaneous manifestation of lethal genes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201638

7 January 2021

Identifiers

DOI

10.1038/SJ.EJHG.5201638

1 reference

PubMed ID

16883308

Dimensions Publication ID

14 August 2017

0 references

1 reference

PubMed ID

16883308