Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1983 1
1984 1
1986 1
1987 4
1988 3
1989 2
1991 2
1992 5
1993 9
1994 4
1995 7
1996 3
1997 5
1998 10
1999 5
2000 8
2001 7
2002 12
2003 7
2004 11
2005 9
2006 8
2007 8
2008 13
2009 10
2010 10
2011 12
2012 13
2013 14
2014 14
2015 5
2016 5
2017 9
2018 9
2019 9
2020 11
2021 11
2022 11
2023 8
2024 3

Text availability

Article attribute

Article type

Publication date

Search Results

278 results

Results by year

Filters applied: . Clear all
Page 1
Proteus syndrome.
Rocha RCC, Estrella MPS, Amaral DMD, Barbosa AM, Abreu MAMM. Rocha RCC, et al. An Bras Dermatol. 2017 Sep-Oct;92(5):717-720. doi: 10.1590/abd1806-4841.20174496. An Bras Dermatol. 2017. PMID: 29166516 Free PMC article.
Proteus syndrome is a rare syndrome characterized by disproportionate overgrowth of limbs, multiple hamartomas, and vascular malformations. ...If present, even alone, they can be considered as a pathognomonic sign. This article reports a classic case of Proteus …
Proteus syndrome is a rare syndrome characterized by disproportionate overgrowth of limbs, multiple hamartomas, and vascular m …
Proteus Syndrome.
Rawal S, Sharma B, Dabla S, Singh J, Goyal S. Rawal S, et al. J Assoc Physicians India. 2016 May;64(5):69-71S. J Assoc Physicians India. 2016. PMID: 27735155
Proteus syndrome is an extremely rare disorder with a documentation of only 100 cases world over till date. This sporadic disorder involves the skeletal system, central nervous system, eyes, skin, soft tissues and vascular system. We report a case of Proteus …
Proteus syndrome is an extremely rare disorder with a documentation of only 100 cases world over till date. This sporadic diso …
Overgrowth syndromes.
Neylon OM, Werther GA, Sabin MA. Neylon OM, et al. Curr Opin Pediatr. 2012 Aug;24(4):505-11. doi: 10.1097/MOP.0b013e3283558995. Curr Opin Pediatr. 2012. PMID: 22705997 Review.
Hemihyperplasia syndromes.
Dalal AB, Phadke SR, Pradhan M, Sharda S. Dalal AB, et al. Indian J Pediatr. 2006 Jul;73(7):609-15. doi: 10.1007/BF02759927. Indian J Pediatr. 2006. PMID: 16877856
RESULTS: Of the 17 cases with hemihyperplasia, 3 cases satisfied the diagnostic criteria for Proteus syndrome. One patient each was ascertained as Klippel Trenaunay Weber syndrome and Hemihyperplasia- Multiple lipomatosis. 9 cases were classified as isolated hemihyp …
RESULTS: Of the 17 cases with hemihyperplasia, 3 cases satisfied the diagnostic criteria for Proteus syndrome. One patient eac …
Genetic basis for vascular anomalies.
Kirkorian AY, Grossberg AL, Püttgen KB. Kirkorian AY, et al. Semin Cutan Med Surg. 2016 Sep;35(3):128-36. doi: 10.12788/j.sder.2016.051. Semin Cutan Med Surg. 2016. PMID: 27607321 Review.
This review summarizes genetic and clinical information on the following diagnoses: capillary malformation, venous malformation, lymphatic malformation, arteriovenous malformation, PIK3CA-related overgrowth spectrum (PROS), Proteus syndrome, SOLAMEN syndrome, Sturge …
This review summarizes genetic and clinical information on the following diagnoses: capillary malformation, venous malformation, lymphatic m …
Encephalocraniocutaneous lipomatosis.
Moog U. Moog U. J Med Genet. 2009 Nov;46(11):721-9. doi: 10.1136/jmg.2009.066068. Epub 2009 Jul 1. J Med Genet. 2009. PMID: 19574261 Review.
BACKGROUND: Encephalocraniocutaneous lipomatosis (ECCL) is a sporadically occurring neurocutaneous disorder of unknown aetiology. It has repeatedly been discussed as a localised form of Proteus syndrome. In 2006, the first large series of patients was reported, and …
BACKGROUND: Encephalocraniocutaneous lipomatosis (ECCL) is a sporadically occurring neurocutaneous disorder of unknown aetiology. It has rep …
Vascular malformations syndromes: an update.
Martinez-Lopez A, Salvador-Rodriguez L, Montero-Vilchez T, Molina-Leyva A, Tercedor-Sanchez J, Arias-Santiago S. Martinez-Lopez A, et al. Curr Opin Pediatr. 2019 Dec;31(6):747-753. doi: 10.1097/MOP.0000000000000812. Curr Opin Pediatr. 2019. PMID: 31693582 Review.
CLOVES syndrome and Klippel-Trenaunay syndrome are PROS disease. Proteus syndrome is an overgrowth syndrome caused by a somatic activating mutation in AKT1. ...
CLOVES syndrome and Klippel-Trenaunay syndrome are PROS disease. Proteus syndrome is an overgrowth syndrome caused by a somati …
Allelic heterogeneity of Proteus syndrome.
Buser A, Lindhurst MJ, Kondolf HC, Yourick MR, Keppler-Noreuil KM, Sapp JC, Biesecker LG. Buser A, et al. Cold Spring Harb Mol Case Stud. 2020 Jun 12;6(3):a005181. doi: 10.1101/mcs.a005181. Print 2020 Jun. Cold Spring Harb Mol Case Stud. 2020. PMID: 32327430 Free PMC article.
Proteus syndrome is a mosaic disorder that can cause progressive postnatal overgrowth of nearly any organ or tissue. To date, Proteus syndrome has been exclusively associated with the mosaic c.49G > A p....
Proteus syndrome is a mosaic disorder that can cause progressive postnatal overgrowth of nearly any organ or tissue. To date, …
Proteus syndrome.
Samlaska CP, Levin SW, James WD, Benson PM, Walker JC, Perlik PC. Samlaska CP, et al. Arch Dermatol. 1989 Aug;125(8):1109-14. Arch Dermatol. 1989. PMID: 2667470 Review.
The term Proteus syndrome was coined in 1983 to describe a disorder of skeletal, hamartomatous, and other mesodermal malformations. ...Including the case reported herein, we have found 34 patients with Proteus syndrome described in the English literatu …
The term Proteus syndrome was coined in 1983 to describe a disorder of skeletal, hamartomatous, and other mesodermal malformat …
Epidermal nevus syndromes.
Sugarman JL. Sugarman JL. Semin Cutan Med Surg. 2007 Dec;26(4):221-30. doi: 10.1016/j.sder.2008.03.006. Semin Cutan Med Surg. 2007. PMID: 18395670 Review.
Several subsets with characteristic features have been delineated including the nevus sebaceous syndrome, Proteus syndrome, CHILD syndrome, Becker nevus syndrome, nevus comedonicus syndrome, and phakomatosis pigmentokeratotica. ...
Several subsets with characteristic features have been delineated including the nevus sebaceous syndrome, Proteus syndrome, CH …
278 results