Mini‐microform cleft lip with complete cleft alveolus and palate: A case report
Cleft lip and cleft alveolus are caused by incomplete fusion of the frontonasal and maxillary prominences. However, milder forms of cleft lip are rarely accompanied by cleft alveolus. Here, we report a rare case of mini‐microform cleft lip with complete cleft alveolus and cleft palate. No findings s...
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Veröffentlicht in: | Congenital anomalies 2021-07, Vol.61 (4), p.133-137 |
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description | Cleft lip and cleft alveolus are caused by incomplete fusion of the frontonasal and maxillary prominences. However, milder forms of cleft lip are rarely accompanied by cleft alveolus. Here, we report a rare case of mini‐microform cleft lip with complete cleft alveolus and cleft palate. No findings suggestive of cleft lip were evident on initial examination. However, three‐dimensional facial measurements confirmed the presence of cleft lip despite no evidence of orbicularis oris muscle (OOM) rupture on ultrasonography. Collapsed nostril, as observed in this case, is usually associated with OOM rupture. However, it can also be caused by skeletal abnormalities, such as cleft alveolus. Three‐dimensional facial measurements and ultrasonography can assist in accurate diagnosis when visual examination is ambiguous. |
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However, milder forms of cleft lip are rarely accompanied by cleft alveolus. Here, we report a rare case of mini‐microform cleft lip with complete cleft alveolus and cleft palate. No findings suggestive of cleft lip were evident on initial examination. However, three‐dimensional facial measurements confirmed the presence of cleft lip despite no evidence of orbicularis oris muscle (OOM) rupture on ultrasonography. Collapsed nostril, as observed in this case, is usually associated with OOM rupture. However, it can also be caused by skeletal abnormalities, such as cleft alveolus. Three‐dimensional facial measurements and ultrasonography can assist in accurate diagnosis when visual examination is ambiguous.</description><identifier>ISSN: 0914-3505</identifier><identifier>EISSN: 1741-4520</identifier><identifier>DOI: 10.1111/cga.12415</identifier><identifier>PMID: 33729631</identifier><language>eng</language><publisher>Kyoto, Japan: John Wiley & Sons Australia, Ltd</publisher><subject>Abnormalities ; Alveoli ; Biomarkers ; Case reports ; cleft alveolus and palate ; Cleft Lip - diagnosis ; Cleft lip/palate ; Cleft Palate - diagnosis ; Disease Management ; facial measurements ; Humans ; Infant ; Infant, Newborn ; Male ; microform cleft lip ; Muscles ; orbicularis oris ; Phenotype ; Physical growth ; Religious missions ; Rupture ; Rupturing ; Short Communication ; Tomography, X-Ray Computed ; Ultrasonic imaging ; Ultrasonography</subject><ispartof>Congenital anomalies, 2021-07, Vol.61 (4), p.133-137</ispartof><rights>2021 The Authors. published by John Wiley & Sons Australia, Ltd on behalf of Japanese Teratology Society</rights><rights>2021 The Authors. Congenital Anomalies published by John Wiley & Sons Australia, Ltd on behalf of Japanese Teratology Society.</rights><rights>2021. This article is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). 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Three‐dimensional facial measurements and ultrasonography can assist in accurate diagnosis when visual examination is ambiguous.</description><subject>Abnormalities</subject><subject>Alveoli</subject><subject>Biomarkers</subject><subject>Case reports</subject><subject>cleft alveolus and palate</subject><subject>Cleft Lip - diagnosis</subject><subject>Cleft lip/palate</subject><subject>Cleft Palate - diagnosis</subject><subject>Disease Management</subject><subject>facial measurements</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Male</subject><subject>microform cleft lip</subject><subject>Muscles</subject><subject>orbicularis oris</subject><subject>Phenotype</subject><subject>Physical growth</subject><subject>Religious missions</subject><subject>Rupture</subject><subject>Rupturing</subject><subject>Short Communication</subject><subject>Tomography, X-Ray Computed</subject><subject>Ultrasonic imaging</subject><subject>Ultrasonography</subject><issn>0914-3505</issn><issn>1741-4520</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>EIF</sourceid><recordid>eNp1kc1KHTEYhoNU9Gi78AYk0I0uRvM3yUwXwuHQqmARoV2HTOYbjWQm02RGcecl9Bp7JU17jtIWms0H-R4e3uRF6ICSE5rPqb01J5QJWm6hBVWCFqJk5A1akJqKgpek3EV7Kd0TwqRUZAftcq5YLTldoJvPbnA_nr_3zsbQhdhj66GbsHcjfnTTHbahHz1MsLk3_gGCnxM2Q4tH480EH_ASW5MARxhDnN6i7c74BO82cx99_fTxy-qiuLo-v1wtrworpCqLqrNW8BaUaWXdUFGrhjW2ZTmYKZVUtuUN1CXlXd0IowizFQMuWltRapgEvo_O1t5xbnpoLQxTNF6P0fUmPulgnP57M7g7fRsedMUloRXLgqONIIZvM6RJ9y5Z8N4MEOakWUkYo6xiIqPv_0HvwxyH_LxMCUUlYZRk6nhN5a9MKUL3GoYS_asonYvSv4vK7OGf6V_Jl2YycLoGHp2Hp_-b9Op8uVb-BDAWnaw</recordid><startdate>202107</startdate><enddate>202107</enddate><creator>Fujiwara, Kumiko</creator><creator>Yoshida, Mitsuna</creator><creator>Nakamichi, Naomi</creator><creator>Saitoh, Satoru</creator><creator>Takaichi, Mayu</creator><creator>Ishizaka, Risa</creator><creator>Tomihara, Kei</creator><creator>Noguchi, Makoto</creator><general>John Wiley & Sons Australia, Ltd</general><general>Wiley Subscription Services, Inc</general><scope>24P</scope><scope>WIN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7TK</scope><scope>7U7</scope><scope>C1K</scope><scope>K9.</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9158-4141</orcidid></search><sort><creationdate>202107</creationdate><title>Mini‐microform cleft lip with complete cleft alveolus and palate: A case report</title><author>Fujiwara, Kumiko ; 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However, milder forms of cleft lip are rarely accompanied by cleft alveolus. Here, we report a rare case of mini‐microform cleft lip with complete cleft alveolus and cleft palate. No findings suggestive of cleft lip were evident on initial examination. However, three‐dimensional facial measurements confirmed the presence of cleft lip despite no evidence of orbicularis oris muscle (OOM) rupture on ultrasonography. Collapsed nostril, as observed in this case, is usually associated with OOM rupture. However, it can also be caused by skeletal abnormalities, such as cleft alveolus. Three‐dimensional facial measurements and ultrasonography can assist in accurate diagnosis when visual examination is ambiguous.</abstract><cop>Kyoto, Japan</cop><pub>John Wiley & Sons Australia, Ltd</pub><pmid>33729631</pmid><doi>10.1111/cga.12415</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0001-9158-4141</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Abnormalities Alveoli Biomarkers Case reports cleft alveolus and palate Cleft Lip - diagnosis Cleft lip/palate Cleft Palate - diagnosis Disease Management facial measurements Humans Infant Infant, Newborn Male microform cleft lip Muscles orbicularis oris Phenotype Physical growth Religious missions Rupture Rupturing Short Communication Tomography, X-Ray Computed Ultrasonic imaging Ultrasonography |
title | Mini‐microform cleft lip with complete cleft alveolus and palate: A case report |
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