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Year Number of Results
1963 2
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1965 1
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1968 2
1969 2
1971 1
1972 1
1973 5
1975 3
1976 2
1977 1
1978 4
1979 2
1980 3
1981 3
1982 3
1983 5
1984 8
1985 4
1986 7
1987 11
1988 10
1989 11
1990 12
1991 19
1992 12
1993 26
1994 23
1995 21
1996 12
1997 19
1998 18
1999 16
2000 19
2001 25
2002 27
2003 19
2004 19
2005 28
2006 24
2007 35
2008 25
2009 19
2010 31
2011 30
2012 34
2013 31
2014 34
2015 36
2016 21
2017 27
2018 29
2019 32
2020 45
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2023 24
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889 results

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Page 1
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. ...Clinical features of this new syndrome are currently being defined. Including the case reported herein, we have found 34 pat …
The term Proteus syndrome was coined in 1983 to describe a disorder of skeletal, hamartomatous, and other mesodermal malformat …
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. ...This article reports a classic case of Proteus syndrome in a 2-year-old male patient who began to show
Proteus syndrome is a rare syndrome characterized by disproportionate overgrowth of limbs, multiple hamartomas, and vas
Proteus syndrome.
Barmakian JT, Posner MA, Silver L, Lehman W, Vine DT. Barmakian JT, et al. J Hand Surg Am. 1992 Jan;17(1):32-4. doi: 10.1016/0363-5023(92)90109-3. J Hand Surg Am. 1992. PMID: 1538109 Review.
Proteus syndrome is a rare congenital disorder that is characterized by a wide variety of deformities including macrodactyly. ...Unlike neurofibromatosis, the soft tissue masses in Proteus syndrome are not nerve tumors but, rather, are hamartomas compo
Proteus syndrome is a rare congenital disorder that is characterized by a wide variety of deformities including macrodactyly.
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
Proteus syndrome review: molecular, clinical, and pathologic features.
Cohen MM Jr. Cohen MM Jr. Clin Genet. 2014 Feb;85(2):111-9. doi: 10.1111/cge.12266. Epub 2013 Oct 23. Clin Genet. 2014. PMID: 23992099 Review.
Proteus syndrome is caused by an activating AKT1 mutation (c.49G>A, p.Glu17Lys). ...
Proteus syndrome is caused by an activating AKT1 mutation (c.49G>A, p.Glu17Lys). ...
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: ocular complications.
Burke JP, Bowell R, O'Doherty N. Burke JP, et al. J Pediatr Ophthalmol Strabismus. 1988 Mar-Apr;25(2):99-102. doi: 10.3928/0191-3913-19880301-12. J Pediatr Ophthalmol Strabismus. 1988. PMID: 3282059 Review.
Proteus syndrome is a recently recognized hamartoneoplastic malformation syndrome of uncertain etiology and variable expression, whose cardinal manifestations are pigmented nevi, hemihypertrophy, macrodactly, lipomata, and cerebroid-gyriform configuration of
Proteus syndrome is a recently recognized hamartoneoplastic malformation syndrome of uncertain etiology and variable ex
Proteus Syndrome: Case Report with Anatomopathological Correlation.
Arredondo Montero J, Bronte Anaut M, López-Gutiérrez JC. Arredondo Montero J, et al. Fetal Pediatr Pathol. 2022 Oct;41(5):861-864. doi: 10.1080/15513815.2021.1989097. Epub 2021 Oct 20. Fetal Pediatr Pathol. 2022. PMID: 34668833
Background: Proteus syndrome is characterized by a progressive segmental or patchy growth of bone, skin, adipose tissue, and central nervous system, associated with a wide range of neoplasms, pulmonary pathology, and thrombotic risk. ...Genetic evaluation confirmed …
Background: Proteus syndrome is characterized by a progressive segmental or patchy growth of bone, skin, adipose tissue, and c …
Proteus Syndrome: A Rare Case in An Adult Ward.
Duarte Santos C, Lizardo Grácio R, Costa Pires T, Gonzalez Santos M, Rodrigues RJ, Magalhães M, Mota Ponte A. Duarte Santos C, et al. Eur J Case Rep Intern Med. 2021 Apr 28;8(4):002554. doi: 10.12890/2021_002554. eCollection 2021. Eur J Case Rep Intern Med. 2021. PMID: 33987133 Free PMC article.
Proteus syndrome is an extremely rare disorder that manifests as an asymmetric, disproportionate overgrowth of any connective tissue, such as bone, fat or epidermal nevi, in a mosaic or patchy pattern. ...The authors present the case of a patient with Proteus
Proteus syndrome is an extremely rare disorder that manifests as an asymmetric, disproportionate overgrowth of any connective
[Proteus syndrome in the practice of an otorhinolaryngologist: a clinical case].
Stozhkova IV, Pchelenok EV, Kosyakov SY. Stozhkova IV, et al. Vestn Otorinolaringol. 2020;85(2):45-48. doi: 10.17116/otorino20208502145. Vestn Otorinolaringol. 2020. PMID: 32476389 Review. Russian.
Described a rare clinical observation of a patient aged 18 years with chronic left-sided otitis media against Proteus syndrome. By this age, the patient underwent a large number of operations regarding the removal of lymphangiomas, hemlimfangiomas, angiokeratitis of …
Described a rare clinical observation of a patient aged 18 years with chronic left-sided otitis media against Proteus syndrome
889 results