Results 11 to 20 of about 1,489 (136)

Síndrome de Fraser: relato de caso nas vias lacrimais [PDF]

open access: yesRevista Brasileira de Oftalmologia, 2014
A síndrome de Fraser é uma condição sistêmica caracterizada por criptoftalmo, sindactilia e anomalia da genitália, podendo se associar com alterações dos rins, do ouvido, do nariz, da laringe e do esqueleto.
Silvia Helena Tavares Lorena   +5 more
doaj   +4 more sources

Surgical techniques for smile restoration in patients with Möbius syndrome. [PDF]

open access: yesJ Clin Exp Dent, 2013
Möbius syndrome is a congenital condition, the etiology when is not associated with misoprostol is not well defined. Signs and symptoms include difficulty swallowing, speech problems, drooling, strabismus, limitation of eye movement and more importantly,
Morales-Chávez M   +2 more
europepmc   +2 more sources

[Translated article] Prospective study about orthopaedic treatment of fifth metacarpal neck fractures

open access: yesRevista Española de Cirugía Ortopédica y Traumatología, 2022
Introduction: The fifth metacarpal neck fracture is traditionally treated with closed reduction and intrinsic plus cast immobilisation. Another alternative and more functional treatment is the syndactylia.
J. Zugasti Marquínez   +5 more
doaj   +1 more source

Fraser syndrome: case report [PDF]

open access: yes, 2008
Fraser syndrome is a systemic condition characterized by cryptophthalmos, syndactyly and abnormal genitalia, which may be associated with urinary tract, ear, nose, larynx and skeletal abnormalities.
Chaves, Alessandra Pinheiro   +4 more
core   +2 more sources

Anomalía de Poland, a propósito de dos casos

open access: yesCiencia y Salud, 2019
Introducción: el síndrome de Poland, conocido también como secuencia de Poland o anomalía de Poland, fue descrito por primera vez por Alfred Poland en 1841.
Rosario Almánzar
doaj   +1 more source

Apert Syndrome: orthopedic treatment [PDF]

open access: yes, 2011
El Síndrome de Apert es un trastorno autosómico dominante, caracterizado por craneosinostosis, hipoplasia del tercio medio de la cara y sindactilia de manos y pies.
Alonso Tajes, Francisco   +3 more
core   +2 more sources

Type 2 Pfeiffer syndrome. Report of a case and review of the literature

open access: yesActa Pediátrica de México, 2014
Pfeiffer syndrome is a rare autosomal dominant disease that affects almost 1 out of every 100,000 live newborns, and it is associated with craniosynostosis, broad and deviated thumbs and big toes, and partial syndactyly in hands and feet.
Roldán Arce Jorge   +1 more
doaj   +1 more source

La discapacidad en la Prehistoria [PDF]

open access: yes, 2013
XVIII Jornades de Foment de la Investigació de la Facultat de Ciències Humanes i Socials (Any 2013)Se analizan algunas malformaciones congénitas y enfermedades que se han documentado en ciertos individuos durante el largo proceso de la Prehistoria ...
Cucala Devís, Marta
core   +1 more source

Plasticity of the human cerebral cortex as revealed by transcranial magnetic stimulation [PDF]

open access: yes, 2004
Um velho dogma da biologia afirma que só existiria capacidade de reorganização cortical (neuroplasticidade) em animais muito jovens; no adulto, tal capacidade seria pequena ou mesmo inexistente.
Brasil Neto, Joaquim Pereira
core   +3 more sources

Bandas de constrição congênitas Congenital constriction bands

open access: yesActa Ortopédica Brasileira, 2001
A síndrome da banda de constrição congênita é uma patologia rara, de ocorrência ocasional na natureza e não existe predisposição genética. É freqüentemente associada a amputações de dedos ou membros, sindactilia, acrossindactilia (sindactilia fenestrada),
Arlindo G. Pardini Jr.   +2 more
doaj   +1 more source

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