Surgical management of intracranial hypertension in rickets-related craniosynostosis by Alessio Iacoangeli, Sergio Capelli, Andrea Held, Emidio Procaccini, Davide Luglietto, Matteo Barba, Alessandro De Benedictis, Carlo Gandolfo, Carlo Efisio Marras

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Atypical Craniosynostosis with Torticollis and Neurological Symptoms: A Rhombencephalosynapsis Sequence by Virve Koljonen, Junnu Leikola, Leena Valanne, Jyri Hukki

“…Our patient presented with atypical craniosynostosis and balance problems, not typical for scaphocephaly. …”
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Post-surgical complications in patients operated of craniosynostosis. Five year study by Miguel Angel Cruz Díaz, Ángel Serafín Camacho Gómez, Carlos Javier Artiles Rivero, Ramón Sarduy Arana

“…Introduction: most corrective surgeries in patients with craniosynostosis are performed without major complications; Despite this, there are factors that negatively influence its correct evolution. …”
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Characterization of patients operated on for non-syndromic craniosynostosis. Villa Clara, 2018-2022 by Miguel Ángel Cruz Díaz, Ángel Serafín Camacho Gómez, Carlos Javier Artiles Rivero, Ramón Sarduy Arana

“…<p><strong>Background</strong>: craniosynostosis is one of the most frequent neurosurgical pathologies in the pediatric age. …”
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Sagittal Craniosynostosis with Uncommon Anatomical Pathologies in a 56-Year-Old Male Cadaver by Andrey Frolov, Craig Lawson, Joshua Olatunde, James T. Goodrich, John R. Martin III

“…Sagittal craniosynostosis (CS) is a pathologic condition that results in premature fusion of the sagittal suture, restricting the transverse growth of the skull leading in some cases to elevated intracranial pressure and neurodevelopmental delay. …”
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Understanding families’ experiences following a diagnosis of non-syndromic craniosynostosis: a qualitative study by Jill Chorney, Victoria Kuta, Lauren Curry, Daniel McNeely, Simon Walling, Michael Bezuhly

“…Objectives Craniosynostosis is typically diagnosed and surgically corrected within the first year of life. …”
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Corrigendum to “Eye Manifestations of Shprintzen–Goldberg Craniosynostosis Syndrome: A Case Report and Systematic Review” by Jamie H. Choi, Rachel Li, Rachel Gannaway, Tahnee N. Causey, Anna Harrison, Natario L. Couser

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A multiple suture craniosynostosis with fusion of sagittal, metopic, and bilateral coronal sutures: Case report by Ozan Başkurt, Hidayet Ş. Çine, Ece Uysal, Tufan Hicdonmez

“… Multisutural synostosis, characterized by the fusion of multiple cranial sutures without a clear underlying syndrome, represents a rare subtype of craniosynostosis. Particularly uncommon is the simultaneous fusion of the sagittal, metopic, and bilateral coronal sutures. …”
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Apert syndrome: a rare congenital anomaly and experience from a low-resource country: a case report and review of the literature by Maimuna Abdatam, Charles John Nhungo, Frank Muhamba, Ally Hamis Mwanga, Larry Akoko, Charles A. Mkony

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The First Cranial Trepanation Find in a Meotian Burial Ground (Starokorsunskiy Settlement No. 2, Krasnodar Region) by Nataliya Ya. Berezina, Aleksandra N. Abramova, Artem K. Avakyan, Aleksei V. Ivanov, Inna L. Marmer, Evgeny Yu. Girya

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Targeted allele-specific FGFR2 knockdown via human recombinant ferritin nanoparticles for personalized treatment of Crouzon syndrome by Federica Tiberio, Martina Salvati, Luca Polito, Giada Tisci, Alessia Vita, Ornella Parolini, Luca Massimi, Lorena Di Pietro, Pierpaolo Ceci, Gianpiero Tamburrini, Alessandro Arcovito, Elisabetta Falvo, Wanda Lattanzi

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Radial, renal and craniofacial anomalies: Baller-Gerold syndrome by Jyotsna Murthy, Ramesh Babu, Padmasani Venkat Ramanan

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Bilateral Severely Stenotic Jugular Foramen: Diagnosis and Management from the Otologist/Neurotologist Point of View by Raquel Acinho Bento, David Rodrigues, João Levy, Tiago Eça, Vitor Oliveira, Leonel Luís

“…Bilateral jugular foramen stenosis with jugular bulb and vein aplasia is rare in nonsyndromic craniosynostosis and usually diagnosed during childhood. …”
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Gene Therapy: A step toward advanced orthodontics – A narrative review by Monika Shukla, Shalu Jain, C. Munish Reddy, Pradeep Raghav, Kumar Amit, Rinchin Yangzom, Shivika Garg, Aastha Kamrani

“…Discussion: Gene therapy was found to have a major role in orthodontics, especially for: (i) Modulation in OTM, (ii) Alleviation of orthodontic pain, (iii) Enhancement of bone repair and regeneration, (iv) Improving midface hypoplasia by preventing syndromic craniosynostosis, and (v) Modifying condylar growth.…”
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Headache in a Child with Pseudohypoparathyroidism: An Alarming Symptom Not to Miss by Sarah Wing-yiu Poon, Brian Hon-yin Chung, Anita Man-ching Tsang, Grace Wing-kit Poon

“…Other associated neurological features reported in pseudohypoparathyroidism type 1a include spinal stenosis, syringomyelia, and craniosynostosis. While less commonly seen, awareness to these associations is important in order to optimize the multidisciplinary care to this group of patients.…”
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Prenatal Identification and Molecular Characterization of Two Simultaneous De Novo Interstitial Duplications of Chromosomal Regions 7p22.1p21.1 and 15q24.1 by Sabrina C. Burn, Kali Swift, Maria Palmquist

“…Postnatal examination of the neonate was significant for low set ears, thick helices, flat nasal bridge, ankyloglossia, and aberrant head shape and size concerning for craniosynostosis. Postnatal MRI was consistent with Dandy-Walker variant showing hypogenesis of the inferior cerebellar vermis. …”
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Detection of inversion with breakpoints in ARSB causing MPS VI by whole-genome sequencing: lessons learned and best practices by Yufeng Huang, Wenyue Deng, Hui Huang, Xiankai Zhang, Xiaohong Chen, Jian Ye, Sukun Luo, Ting Yu, Hui Yao, Hao Du, Xuelian He

“…Usually, whole exome sequencing (WES) can identify these variants, and if WES failed to detect causative variants, whole-genome sequencing (WGS) may be considered to investigate deep intronic variations and structural alterations in patients.MethodsWhole-exome sequencing (WES) and whole genome sequencing (WGS) were performed in a Chinese family having a boy with suspected diagnosis of MPS with macrocephaly, coarse facial features, broad forehead, thick lips, frontal bossing, craniosynostosis, blue spots, frequent upper respiratory infections, inguinal hernia, and dysostosis multiplex. …”
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