Auricular Cartilage Grafting for Lower-Eyelid Entropion in Syndromic Craniosynostosis: A Case Series
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
A Second Report of a Missense Variant in AMMECR1 Causing Midface Hypoplasia, Hearing Impairment, Elliptocytosis, and Nephrocalcinosis: Case Report and Literature Review. [PDF]
Tan JW +10 more
europepmc +1 more source
[[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]
Sun Z +11 more
europepmc +1 more source
Cranial Base Changes After Trans-sutural Distraction Osteogenesis in Growing Patients With Cleft Lip/Palate and Midface Hypoplasia. [PDF]
Zhou B, Li G, Zhang P, Zhao Z.
europepmc +1 more source
A3-Mandibular Prognathism and Vertical Maxillary Deficiency (Class III)
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]
Gatsis A +8 more
europepmc +1 more source
Apert Syndrome: Oral, Maxillofacial and Dental Management-A Narrative Clinical Review. [PDF]
Kolomvos NGA, Papadaki T, Venetis G.
europepmc +1 more source
Case Report - The Antley-Bixler Syndrome: Two New Cases
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]
Jares Baglivo S +4 more
europepmc +1 more source

