Results 31 to 40 of about 19,555 (135)

Fronto-temporal cerebriform connective tissue nevus in Proteus syndrome

Indian Journal of Dental Research, 2014
Proteus syndrome is one of the very rare syndromes with occurrence of cerebriform connective tissue nevus. The aim of the present manuscript was to present a case of Proteus syndrome in an unusual facial location, which to the best of our knowledge, is ...
S M Balaji
doaj   +1 more source

Mutation in Genes FBN1, AKT1, and LMNA: Marfan Syndrome, Proteus Syndrome, and Progeria Share Common Systemic Involvement

International Journal of Medical Students, 2015
Genetic mutations are becoming more deleterious day by day. Mutations of Genes named FBN1, AKT1, LMNA result specific protein malfunction that in turn commonly cause Marfan syndrome, Proteus syndrome, and Progeria, respectively.
Tonmoy Biswas
doaj   +1 more source

Proteus Syndrome in the minimal form

Journal of the Foot & Ankle, 2020
This is the case report involving a 14-year-old male patient with Proteus syndrome. In an outpatient consultation, the patient complained of pain in the right foot on exertion. On physical examination, the findings were gigantism observed through lateral
Caroline Cunico, João Luis Vieira da Silva, Leonardo Mugnol, Rosangela Alquieri Fedato, Luiz Antonio Munhoz da Cunha   +4 more
doaj   +1 more source

Dysplastic Foot with Soft-Tissue Hypertrophy: Radiographic Features Suggestive of Proteus Syndrome

Radiography Open
Introduction: Proteus syndrome is a rare, sporadic, and highly variable disorder characterized by asymmetric and disproportionate overgrowth of multiple tissues, including bone, skin, and adipose tissue.
Debabrata Maitra
doaj   +1 more source

Radiographic findings of Proteus Syndrome

Radiology Case Reports, 2014
The extremely rare Proteus Syndrome is a hamartomatous congenital syndrome with substantial variability between clinical patient presentations. The diagnostic criteria consist of a multitude of clinical findings including hemihypertrophy, macrodactyly ...
Nishant Mukesh Gandhi, MD, Eric A. Davalos, MD, Rajeev K. Varma, MD   +2 more
doaj   +1 more source

Bronchoscopic concerns in Proteus syndrome: a case report [PDF]

Korean Journal of Anesthesiology, 2016
Proteus syndrome (PS) is a rare congenital hamartomatous disorder with multisystem involvement. PS shows highly clinical variability due to overgrowth of the affected areas, and several features can make anesthetic management challenging. Little is known
Jung-Min Hong, Hyeon Jeong Lee, Eun Soo Kim, Hae-Kyu Kim, Soeun Jeon, Hyae-Jin Kim   +5 more
doaj   +1 more source

[Proteus syndrome].

Der Hautarzt; Zeitschrift fur Dermatologie, Venerologie, und verwandte Gebiete, 1991
Proteus syndrome is a rare congenital disorder in which the major clinical manifestations are skeletal deformities and hamartomatous tumors. The case of a 42-year-old woman with right hemihypertrophy, macrodactyly of the right hallux, extreme kyphoscoliosis and bilateral plantar connective tissue naevi is reported.
D, Maassen, V, Voigtländer
  +6 more sources

Proteus syndrome [PDF]

Atlas of Genetics and Cytogenetics in Oncology and Haematology, 2011
Review on Proteus syndrome, with data on clinics, and the genes involved.
Choyke, PL, Biesecker, LG
openaire   +2 more sources

A Case of Proteus Syndrome with Hemangioma Presentation

Journal of Clinical and Basic Research, 2018
Background: Proteus syndrome is a rare genetic disorder characterized by overgrowth of bones, skin, and other tissues, with vascular malformations, epidermal moles, and subcutaneous masses.
Jabbar Parhiz, Atefeh Kami, Narges Lashkarbolouk, Hamid Soltani Pasha   +3 more
doaj   +2 more sources

Unilateral hypertrophic skin lesions, hemimegalencephaly, and meningioma: The many faces of Proteus syndrome

Indian Dermatology Online Journal, 2015
Proteus syndrome is a rare condition with a wide spectrum of abnormalities. It is characterized by hamartomatous malformations involving multiple organs.
Niharika R Lal, Debabrata Bandyopadhyay, Asim K Sarkar   +2 more
doaj   +1 more source