Results 111 to 120 of about 1,158,693 (154)
Scandinavian Journal of Plastic and Reconstructive Surgery and Hand Surgery, 2003 Proteus syndrome is a rare sporadic, hamartoneoplastic disorder of vascular, skeletal, and soft tissues that causes asymmetry of the skull, body, arms, and the legs. The name "Proteus" of the Greek god who had the ability to change his shape was coined to define the variety of deformities including partial gigantism of the hands or feet, asymmetry of ...
Cuneyt Özek, Ufuk Bilkay
exaly +4 more sources
Annals of Plastic Surgery, 2002 Proteus syndrome is a very rare congenital condition comprising malformations and overgrowth of multiple sorts of tissue. It was described for the first time in 1979 and was termed Proteus syndrome in 1983. The authors describe a 37-year-old patient who was diagnosed initially as having Klippel-Trenaunay-Weber syndrome at the age of 10 years.
Edwin, Müller +2 more
core +4 more sources
Anesthesia for proteus syndrome
Pediatric Anesthesia, 2004 SummaryProteus syndrome is a complex disorder comprising malformations and overgrowth of multiple tissues. The disorder is highly variable affecting tissues in a mosaic pattern. A 2‐year‐old boy with Proteus syndrome, with epidermal verrucal naevus, hyperplastic lesions of connective tissue, hyperostosis, overgrowth of tubular bones, bilateral inguinal
Gungor, İRFAN +4 more
openaire +4 more sources
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Pediatric Dermatology, 1989
The term Proteus syndrome was coined in 1983 to describe a disorder of skeletal, hamartomatous, and other mesodermal malformations. The syndrome was named after the Greek god Proteus, whose name means "the Polymorphous." Clinical features of this new syndrome are currently being defined.
T, Costa, B R, Krafchik
+6 more sources
The term Proteus syndrome was coined in 1983 to describe a disorder of skeletal, hamartomatous, and other mesodermal malformations. The syndrome was named after the Greek god Proteus, whose name means "the Polymorphous." Clinical features of this new syndrome are currently being defined.
T, Costa, B R, Krafchik
+6 more sources
Severe gynaecological involvement in Proteus Syndrome
European Journal of Medical Genetics, 2019 IF 2.004International audienceProteus Syndrome is a rare complex overgrowth syndrome. We report a young female patient with Proteus Syndrome due to AKT1 mutation c.49G > A (p.Glu17Lys), presenting with a severe gynaecological involvement which ...
Laurence Faivre, Nicolas Chassaing
exaly +2 more sources
Pediatric Dermatology, 1994
Abstract: A 10‐month‐old girl had macrodactyly, facial and extremity hemihypertrophy, plantar cerebriform hyperpiasia, a subcutaneous mass on the back, macrocephaly, and lumbar kyphosis. These findings were diagnostic of Proteus syndrome. The clinical features, etiology, management, and points of differential diagnosis are discussed.
G L, Darmstadt, A T, Lane
openaire +4 more sources
Abstract: A 10‐month‐old girl had macrodactyly, facial and extremity hemihypertrophy, plantar cerebriform hyperpiasia, a subcutaneous mass on the back, macrocephaly, and lumbar kyphosis. These findings were diagnostic of Proteus syndrome. The clinical features, etiology, management, and points of differential diagnosis are discussed.
G L, Darmstadt, A T, Lane
openaire +4 more sources
Dermatology, 2001
A case of Proteus syndrome is presented, in which severe hemihypertrophy of the left trunk and left lower extremity, scoliosis, endometriosis and huge bizarre-shaped body tumors were observed. Up to 22.6 kg of tumorous tissue was excised. This syndrome was first described in 1983.
H, Yasuda +5 more
openaire +4 more sources
A case of Proteus syndrome is presented, in which severe hemihypertrophy of the left trunk and left lower extremity, scoliosis, endometriosis and huge bizarre-shaped body tumors were observed. Up to 22.6 kg of tumorous tissue was excised. This syndrome was first described in 1983.
H, Yasuda +5 more
openaire +4 more sources
Vasa, 2003
A 34-year-old male patient was referred with a recalcitrant leg ulcer overlying an extensive vascular malformation, which had led several times to septic soft tissue infections. During his infancy he had been diagnosed to have Klippel-Trenaunay syndrome.
G, Dragieva +6 more
openaire +3 more sources
A 34-year-old male patient was referred with a recalcitrant leg ulcer overlying an extensive vascular malformation, which had led several times to septic soft tissue infections. During his infancy he had been diagnosed to have Klippel-Trenaunay syndrome.
G, Dragieva +6 more
openaire +3 more sources
International Journal of Dermatology, 2000
A 7‐year‐old girl presented with a history of wine‐colored tumoral lesions on her leg, right foot, abdomen, and back, present since birth. They bled easily on touch or on minimal trauma. Soft, skin‐colored tumors were also present on the pectoral and left axillary regions. All the lesions had increased in size gradually.
J A, Cavero, E G, Castro, L, Junco
openaire +2 more sources
A 7‐year‐old girl presented with a history of wine‐colored tumoral lesions on her leg, right foot, abdomen, and back, present since birth. They bled easily on touch or on minimal trauma. Soft, skin‐colored tumors were also present on the pectoral and left axillary regions. All the lesions had increased in size gradually.
J A, Cavero, E G, Castro, L, Junco
openaire +2 more sources