Apert Syndrome: A Case Report by Shahin Mafinejad, Hojat Ehteshammanesh, Ghasem Bayani, Hosein Mahmoodzade

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A rare case of stickler marshall syndrome by Bharat Gurnani, Kirandeep Kaur

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Smith-Magenis Syndrome: Self-Hugging Behavior by J Gordon Millichap

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Craniofacial manifestations and dental considerations in association with achondroplasia: Clinical insight and report of a case by Nidhi Chhabra, Anuj Chhabra, Ruchi Mehta

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Craniosynostosis in Siblings, an Extremely Rare Occurrence: A Case Report by Tirth Bhavsar, Sachin Mahendrakumar Chaudhary, Sumesh Singh

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Clinical Features in Patients with Xq23 Microdeletion: A Case Report and Literature Review by Lu Qin, Fei-Zhou Zhang, Jian-Hai Lv, Lan-Fang Tang

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Apert syndrome by Premalatha, Kannan V, Madhu

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Aberrant growth of the anterior cranial base relevant to severe midface hypoplasia of Apert syndrome by Bong Kuen Cha, Dong Soon Choi, In San Jang, Hyun Tae Yook, Seung Youp Lee, Sang Shin Lee, Suk Keun Lee

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Less invasive treatment of sleep-disordered breathing in children with syndromic craniosynostosis by Silvia Müller-Hagedorn, Cornelia Wiechers, Jörg Arand, Wolfgang Buchenau, Margit Bacher, Michael Krimmel, Siegmar Reinert, Christian F. Poets

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Midface advancement in an adult patient with Crouzon syndrome: Modified LeFort III + LeFort I osteotomy accompanied by genioplasty and nasal dorsum augmentation by Milad Etemadi Sh, Golnaz Tajmiri

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Assessment of Soft Tissue Changes after Various Orthognathic Surgeries for Class III Correction of Cleft Lip and Cleft Palate Patients: A Systematic Review and Meta-Analysis by B Kanagasabapathy, Shubham Sharma, Piyush Dua, Nikil K. Jain, V Preethi, Monika

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Novel mutation in the COL11A1 gene causing Marshall-Stickler syndrome in three generations of a Bulgarian family by Mladenova M, Todorov T, Grozdanova L, Mitev V, Todorova A

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