Results 21 to 30 of about 1,158,693 (154)

Proteus syndrome

open access: yesThe Journal of Hand Surgery, 1992
Proteus syndrome is a rare congenital disorder that is characterized by a wide variety of deformities including macrodactyly. Skin and soft tissue lesions are common; they may increase in size as the child develops and may assume tremendous proportions.
J T, Barmakian   +4 more
openaire   +3 more sources

Proteus syndrome

open access: yesIndian Journal of Dermatology, Venereology and Leprology, 2005
Proteus syndrome is a variable and complex disorder characterized by multifocal overgrowths affecting any tissue or structure of the body. We present a girl aged 3 years and 8 months with an epidermal nevus, port-wine stain, macrodactyly with gigantism of the feet, lymphohemagiomas and multiple lipomas.
Basanti, Debi   +3 more
openaire   +2 more sources

Proteus syndrome: presenting as a large ovarian cyst [PDF]

open access: yesNew Indian Journal of OBGYN, 2020
Abnormal huge progressive enlargement and fusion of digits with limitation of joint movements (macrodactyly, syndactyly, and arthrogryposis) are usually part of a syndromic manifestation.
Amita Ray   +3 more
doaj   +1 more source

Sinonasal Neuroendocrine Carcinoma in Adult Proteus Syndrome [PDF]

open access: yesIranian Journal of Otorhinolaryngology, 2023
Introduction:Proteus syndrome (PS) is a rare genetic disorder usually caused by mutations in AKT1 or PTEN genes, characterized by multiple, asymmetric tissue overgrowth with high clinical variability.
Giorgos Sideris   +5 more
doaj   +1 more source

Sirolimus treatment of a PTEN hamartoma tumor syndrome presenting with melena

open access: yesThe Turkish Journal of Pediatrics, 2022
Background. PTEN hamartoma tumor syndrome (PHTS) is an umbrella term including Cowden syndrome (CS), Bannayan-Riley-Ruvalcaba syndrome (BRRS), PTEN-related Proteus syndrome (PS), and PTEN-related Proteus-like syndrome. One of the disorders in PHTS
Gülseren Evirgen Şahin   +5 more
doaj   +1 more source

Endometrioid Paraovarian Borderline Cystic Tumor in an Infant with Proteus Syndrome

open access: yesCase Reports in Oncological Medicine, 2015
Ovarian and paraovarian neoplasms are uncommon in children, mainly originating from germ cell tumors and, least frequently, epithelial tumors. There is an association between genital tract tumors and Proteus syndrome, a rare, sporadic, and progressive ...
Liliana Vasquez   +6 more
doaj   +1 more source

Proteus Syndrome: A Natural Clinical Course of Proteus Syndrome

open access: yesYonsei Medical Journal, 2002
A 16-year-old Korean male patient presented with macrodactyly, hemihypertrophy of the face and extremities, plantar cerebriform hyperplasia, a subcutaneous mass of the left chest, macrocephaly and verrucous epidermal nevi. These findings are consistent with Proteus Syndrome.
John A, Linton   +2 more
openaire   +2 more sources

Unilateral proteus syndrome in a neonate: A very rare presentation

open access: yesIndian Journal of Paediatric Dermatology, 2016
Proteus syndrome (PS) is a rare sporadic disorder with postnatal asymmetric overgrowth from any of the three germinal layers. The tissue overgrowth may present at birth but becomes more conspicuous with the progression of age.
Chinmay Kar   +4 more
doaj   +1 more source

Germline mutations in the oncogene EZH2 cause Weaver syndrome and increased human height [PDF]

open access: yes, 2011
The biological processes controlling human growth are diverse, complex and poorly understood. Genetic factors are important and human height has been shown to be a highly polygenic trait to which common and rare genetic variation contributes.
Tatton-Brown, Katrina   +57 more
core   +2 more sources

Estudio de la biosíntesis del núcleo de lipopolisacarido (LPS) en "Proteus mirabilis" [PDF]

open access: yes, 2013
[eng] Urinary tract infection (UTIs) is an extremely common disease. Proteus mirabilis is a common cause of UTI in individuals with functional or structural abnormalities or with long-term catheterization, it forms bladder and kidney stones as a ...
Aquilini, Eleonora
core   +4 more sources

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