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

