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Radiological Imaging in Diagnosis of Proteus Syndrome [PDF]
Journal of Clinical and Diagnostic Research, 2019 Proteus syndrome is a rare hamartomatous condition with multisystem involvement and diverse clinical manifestations, common ones being hemihypertrophy of one or more body parts, presence of lipomas, cutaneous epidermal nevi and vascular malformations ...
Shibani Mehra +2 more
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Proteus syndrome: presenting as a large ovarian cyst [PDF]
New 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
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Sirolimus treatment of a PTEN hamartoma tumor syndrome presenting with melena
The 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
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Proteus syndrome: a case report with bone scintigraphy findings
Diagnostic and Interventional Radiology, 2013 Proteus syndrome is an extremely rare genetic disorder characterized by an asymmetrical overgrowth of skin, bones, muscles, fatty tissues, and blood and lymphatic vessels.
Bangkim Chandra Khangembam +7 more
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Indian 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
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Endometrioid Paraovarian Borderline Cystic Tumor in an Infant with Proteus Syndrome
Case 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
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Proteus Syndrome: A Natural Clinical Course of Proteus Syndrome
Yonsei 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
Indian 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
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Proteus syndrome in a child aged 14 years and 11 months
Alʹmanah 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
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Pulmonary Manifestations and Management of Proteus Syndrome
Journal of the Formosan Medical Association, 2010 Proteus syndrome is a very rare, sporadic and congenital condition that is characterized by postnatal mosaic overgrowth. This disorder is thought to be caused by a somatic gene mutation, but the exact etiology is unknown.
Chia-Ying Li +3 more
doaj +1 more source