Results 111 to 120 of about 28,866 (195)

Auricular Cartilage Grafting for Lower-Eyelid Entropion in Syndromic Craniosynostosis: A Case Series

open access: yes
Patients with syndromic craniosynostosis, including Crouzon and Pfeiffer syndromes, may develop lower-eyelid malposition, including retraction and secondary entropion, associated with complex midfacial and orbital anatomical abnormalities.
Akimitsu Sato   +4 more
core   +1 more source

Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings

open access: yes, 2012
[[abstract]]"Objective: To present prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 1p (1p36.23 pter) and partial trisomy 20p (20p12.1 pter) associated with ventriculomegaly, ventricular septal defect and midface ...
陳持平;Chen, Chih-Ping;Chen, Ming;Su, Yi-Ning;Hsu, Chin-Yuan;Tsai, Fuu-Jen;Chern, Schu-Rern;Wu, Pei-Chen;Lee, Chen-Chi;Wang, Wayseen
core  

Mechanical force-induced oncostatin M secretion by Jun-positive neutrophils promotes craniofacial bone regeneration for midface hypoplasia treatment. [PDF]

open access: yesStem Cell Res Ther
Sun Z   +11 more
europepmc   +1 more source

A3-Mandibular Prognathism and Vertical Maxillary Deficiency (Class III)

open access: yes
Sagittal mandibular prognathism (mandibular excess) as basic deviation may occur in combination with various maxillary deformities: + Sagittal maxillary deficiency (maxillary retrognathism/midface hypoplasia) Vertical maxillary excess (VME) Vertical ...
Lie, Suen An Nynke   +2 more
core   +1 more source

Kabuki Syndrome: Case Report of Severe Prenatal Midface Hypoplasia (Binder Phenotype), due to a Novel Variant in the <i>KMT2D</i> Gene. [PDF]

open access: yesMol Syndromol
Gatsis A   +8 more
europepmc   +1 more source

Case Report - The Antley-Bixler Syndrome: Two New Cases

open access: yes, 2002
The Antley-Bixler syndrome is a rare multiple congenital anomaly with a high mortality rate. The characteristic manifestations include craniosynostosis, radiohumeral synostosis, midface hypoplasia, joint contractures and arachnodactyly. We report two new
Hosalkar HS, Shah HS, Gujar PS, Shaw BA
core  

Liveborn trisomy 22: a case report. [PDF]

open access: yesFront Pediatr
Jares Baglivo S   +4 more
europepmc   +1 more source

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