Results 31 to 40 of about 1,158,693 (154)

Unilateral proteus syndrome

open access: yesIndian Journal of Dermatology, Venereology and Leprology, 2005
Proteus syndrome is a complex developmental abnormality. It is characterized by both hypertrophic and hypoplastic changes. Deformities have been occasionally found to be localized in one half of the body in head or digit but presence of all signs in one half of the body in a wide spread manner is not reported in the literature.
Nilendu Sarma   +2 more
openaire   +2 more sources

Hemispherectomy Procedure in Proteus Syndrome [PDF]

open access: yes, 2016
How to Cite This Article: Gunawan PI, Lusiana L, Saharso D. Hemispherectomy Procedure in Proteus Syndrome. Iran J Child Neurol.Summer 2016; 10(3):86-90 ObjectiveProteus syndrome is a rare overgrowth disorder including bone, soft tissue, and skin. Central
Lusiana   +5 more
core   +1 more source

Cardiothoracic imaging findings of Proteus syndrome

open access: yesScientific Reports, 2021
In this work, we sought to delineate the prevalence of cardiothoracic imaging findings of Proteus syndrome in a large cohort at our institution. Of 53 individuals with a confirmed diagnosis of Proteus syndrome at our institution from 10/2001 to 10/2019 ...
S. Mojdeh Mirmomen   +6 more
doaj   +1 more source

Proteus syndrome with progressive paralysis of the unilateral lower limb: A rare case report and literature review

open access: yesHeliyon
Objective: Proteus syndrome, a rare disorder with an incidence of one in a million, is characterized by connective tissue nevi, asymmetric limb overgrowth, and abnormal subcutaneous adipose tissue distribution.
Feng Cai   +9 more
doaj   +1 more source

Fronto-temporal cerebriform connective tissue nevus in Proteus syndrome

open access: yesIndian 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

Klippel‐Trénaunay‐Weber Syndrome: Prenatal Diagnosis and Review of the Literature

open access: yesJournal of Clinical Ultrasound, Volume 53, Issue 3, Page 535-546, March/April 2025.
This meta‐analysis demonstrates the high diagnostic accuracy of SZ‐CEUS for differentiating between malignant and benign focal liver lesions, as well as for HCC from non‐HCC lesions. The study shows better performance for smaller lesions and those with a higher proportion of malignancy.
Giuliana Orlandi   +13 more
wiley   +1 more source

A study of urinary catheter encrustation in patients with Proteus urinary tract infection. [PDF]

open access: yes, 2007
The most common cause of encrustation and blockage of long term urinary catheters is colonisation of the urinary tract by Proteus spp. However, the degree of encrustation experienced by those with Proteus colonisation differs markedly between ...
Mathur, S.
core  

Anaesthesia for Proteus syndrome

open access: yesEuropean Journal of Anaesthesiology, 2000
A 4-month-old boy with Proteus syndrome underwent a successful operation for a left abdominal mass due to hydroureter and hydronephrosis with left ureterovesical stenosis. The operation lasted 4.5 h under general anaesthesia; there were no anaesthetic complications. There is only one previous report on anaesthesia in a patient with Proteus syndrome.
A, Ceyhan   +5 more
openaire   +3 more sources

Microbial communities and functional diversity in seafood

open access: yesJSFA reports, EarlyView.
Abstract Functional diversity encompasses ecosystem processes that enhance adaptability to environmental change. This study explores the diversity of microorganisms associated with seafood. In this paper, we present our knowledge of microbial diversity in relation to seafood.
Christian Larbi Ayisi   +3 more
wiley   +1 more source

Proteus syndrome in a child aged 14 years and 11 months

open access: yesAlʹmanah Kliničeskoj Mediciny, 2017
Proteus syndrome is an extremely rare genetic disorder with problematic genetic identification. It has been hypothesized that it is related to a lethal dominant somatic mutation occurring at a post-zygotic stage of embryonic development.
T. V. Elizarova   +5 more
doaj   +1 more source

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