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The role of micro-anchor devices in medial canthopexy
(LIPPINCOTT WILLIAMS & WILKINS, 2008)
Telecanthus, the lateral displacement of the medial canthus, can be a congenital deformity or can occur after facial trauma or tumor resection. Treatment of telecanthus remains a challenge for plastic surgeons. For proper ...
Barber-Say syndrome: further delineation of the clinical spectrum
(Sociedade Brasileira de Genética, 2000)
We report on a 14-year-old girl who presented a multiple congenital anomaly pattern: ablepharon, hypertelorism, telecanthus, macrostomia, helix agenesis of both ears, redundant thick skin and severe hirsutism, the 5th ...
MICHELS SYNDROME IN A BRAZILIAN GIRL BORN TO CONSANGUINEOUS PARENTS
(Wiley-Blackwell, 1995-07-03)
We report on a Brazilian girl born to consanguineous parents and presenting with craniosynostosis, telecanthus, blepharophimosis, blepharoptosis, epicanthus inversus, cleft lip and palate, skeletal defects, and hearing ...
MICHELS SYNDROME IN A BRAZILIAN GIRL BORN TO CONSANGUINEOUS PARENTS
(Wiley-Blackwell, 1995-07-03)
We report on a Brazilian girl born to consanguineous parents and presenting with craniosynostosis, telecanthus, blepharophimosis, blepharoptosis, epicanthus inversus, cleft lip and palate, skeletal defects, and hearing ...
MICHELS SYNDROME IN A BRAZILIAN GIRL BORN TO CONSANGUINEOUS PARENTS
(Wiley-Blackwell, 2014)
Novel mutations of PAX3, MITF and SOX10 genes found in Waardenburg syndrome types 1 and 2 in Brazilian patients
(Sociedade Brasileira de Genática - SBGÁguas de Lindóia, 2013-09-16)
Waardenburg syndrome (WS) is a dominant inherited disorder characterized by pigmentary abnormalities of the skin
and iris (heterochromia or hypochromia irides) associated with sensorial hearing loss and cranio-facial ...
Guadalajara camptodactyly type III: A new probably autosomal dominant syndrome
(2002)
A Mexican family is presented with the main clinical features of camptodactyly, a distinctive facial appearance because of ocular hypertelorism, telecanthus, symblepharon and spinal defects. Other clinical manifestations ...
Guadalajara camptodactyly type III: A new probably autosomal dominant syndrome
(2002)
A Mexican family is presented with the main clinical features of camptodactyly, a distinctive facial appearance because of ocular hypertelorism, telecanthus, symblepharon and spinal defects. Other clinical manifestations ...
Guadalajara camptodactyly type III: A new probably autosomal dominant syndrome
(2014)
High-content screening led to the identification of the N-isobutylamide guineensine from Piper nigrum as novel nanomolar inhibitor (EC50 = 290 nM) of cellular uptake of the endocannabinoid anandamide (AEA). Noteworthy, ...