Imaging of Pfeiffer Syndrome: A Case Report
DOI:
https://doi.org/10.3889/oamjms.2022.9424Keywords:
Case report, Craniosynostosis Pfeiffer syndrome, Radiology, Midface hypoplasiaAbstract
BACKGROUND: Pfeiffer syndrome (PS) is a rare case in the Asian population, and only a few have been reported in Indonesia. This case report aims to spotlight the identification of PS with its correlated radiological imaging and distinguish it from other syndromes.
CASE REPORTS: The authors report a case of a 5-year-old girl with PS, manifested by brachyturricephally, broad thumbs and big toes, and medially deviated big toes. The patient also had proptosis, midface hypoplasia, and bilateral Syndactyly of the fingers and toes. This report confirms the thorough examination procedures and indexes to identify PS as a literature reference for the research of reported PS in Southeast Asian race patients and as one comprehensive source for identification using index figures.
CONCLUSION: This report provides a detailed radiology interpretation of PS on Southeast Asian race patients. Radiological findings can help in diagnosing and determining adequate treatment as needed.Downloads
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Ko JM. Genetic syndromes associated with craniosynostosis. J Korean Neurosurg Soc. 2016;59(3):187-91. https://doi.org/10.3340/jkns.2016.59.3.187 PMid:27226847 DOI: https://doi.org/10.3340/jkns.2016.59.3.187
Vogels A, Fryns JP. Pfeiffer syndrome. Orphanet J Rare Dis. 2006;1:19. https://doi.org/10.1186/1750-1172-1-19 PMid:16740155 DOI: https://doi.org/10.1186/1750-1172-1-19
Pindrik J, Molenda J, Uribe-Cardenas R, Dorafshar AH, Ahn ES. Normative ranges of anthropometric cranial indices and metopic suture closure during infancy. J Neurosurg Pediatr. 2016;25(6):667-73. https://doi.org/10.3171/2016.5.PEDS14336 PMid:27589596 DOI: https://doi.org/10.3171/2016.5.PEDS14336
Dlouhy BJ, Menezes AH. Hydrocephalus in chiari malformations and other craniovertebral junction abnormalities. In: Cinalli G, Ozek MM, Sainte-Rose C, editors. Pediatric Hydrocephalus. Cham: Springer International Publishing; 2018. p. 1119-32. DOI: https://doi.org/10.1007/978-3-319-27250-4_66
Tan AP, Mankad K. Apert syndrome: Magnetic resonance imaging (MRI) of associated intracranial anomalies. Childs Nerv Syst. 2018;34:205-16. https://doi.org/10.1007/s00381-017-3670-0 PMid:29198073 DOI: https://doi.org/10.1007/s00381-017-3670-0
Jullabussapa N, Khwanngern K, Pateekhum C, Angkurawaranon C, Angkurawaranon S. CT-based measurements of facial parameters of healthy children and adolescents in Thailand. AJNR Am J Neuroradiol. 2020:41(10):1937-42. https://doi.org/10.3174/ajnr.A6731 PMid:32855189 DOI: https://doi.org/10.3174/ajnr.A6731
Burns NS, Iyer RS, Robinson AJ, Chapman T. Diagnostic imaging of fetal and pediatric orbital abnormalities. AJAR Am J Roentgenol. 2013:201(6):W797-808. https://doi.org/10.2214/AJR.13.10949 PMid:24261386 DOI: https://doi.org/10.2214/AJR.13.10949
Mathijssen IM. Guideline for care of patients with the diagnoses of craniosynostosis: Working group on craniosynostosis. J Craniofac Surg. 2015:26(6):1735-807. https://doi.org/10.1097/SCS.0000000000002016 PMid:26355968 DOI: https://doi.org/10.1097/SCS.0000000000002016
Šebová I, Vyrvová I, Barkociová J. Nasal cavity CT imaging contribution to the diagnosis and treatment of choanal atresia. Medicina (Kaunas). 2021:57(2):93. https://doi.org/10.3390/medicina57020093 PMid:33494264
Couloigner V, Ayari Khalfallah S. Craniosynostosis and ENT. Neurochirurgie. 2019:65(5):318-21. https://doi.org/10.1016/j.neuchi.2019.09.015 PMid:31568777
Šebová I, Vyrvová I, Barkociová J. Nasal Cavity CT Imaging Contribution to the Diagnosis and Treatment of Choanal Atresia. Medicina (Kaunas). 2021;57(2):93. https://doi.org/10.3390/ medicina57020093 PMid: 33494264 DOI: https://doi.org/10.3390/medicina57020093
Couloigner V, Ayari Khalfallah S. Craniosynostosis and ENT. Neurochirurgie. 2019;65(5):318-21. https://doi.org/10.1016/j.neuchi.2019.09.015 PMid: 31568777 DOI: https://doi.org/10.1016/j.neuchi.2019.09.015
Cohen MM. Apert, crouzon, and pfeiffer syndromes. Monogr Hum Genet. 2011;19(1):67-88. https://doi.org/10.1159/000320211 DOI: https://doi.org/10.1159/000320211
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Copyright (c) 2022 Deni Setiawan, Audy Sarah Putrini Adibrata, Puspita P. Sari, Atta Kuntara, Gery P. Yogaswara (Author)
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