Laryngeal and tracheal anomalies in an infant with oral-facial-digital syndrome type VI (Váradi-Papp): report of a transitional type
The oral-facial-digital syndromes (OFDS) comprise a group of disorders involving malformations of the mouth, face, and digits. There are 13 subtypes of the OFDS, and much overlap exists among OFDS patients. Distinct syndromes such as Joubert and Pallister-Hall display many of the same features. This...
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Veröffentlicht in: | Pediatric radiology 2008-09, Vol.38 (9), p.994-998 |
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description | The oral-facial-digital syndromes (OFDS) comprise a group of disorders involving malformations of the mouth, face, and digits. There are 13 subtypes of the OFDS, and much overlap exists among OFDS patients. Distinct syndromes such as Joubert and Pallister-Hall display many of the same features. This report describes an infant with abnormalities including a hypoplastic/absent cerebellar vermis and forked third metacarpals, consistent with a diagnosis of OFDS type VI (Váradi-Papp). The girl’s abnormalities also included malformations of the larynx and trachea, findings never before described in type VI but described in other OFDS subtypes and similar syndromes. Our patient represents a transitional OFDS type, further supporting evidence of a common molecular pathway among these disorders. This report highlights the importance of the radiologist’s role in diagnosis. |
doi_str_mv | 10.1007/s00247-008-0877-y |
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There are 13 subtypes of the OFDS, and much overlap exists among OFDS patients. Distinct syndromes such as Joubert and Pallister-Hall display many of the same features. This report describes an infant with abnormalities including a hypoplastic/absent cerebellar vermis and forked third metacarpals, consistent with a diagnosis of OFDS type VI (Váradi-Papp). The girl’s abnormalities also included malformations of the larynx and trachea, findings never before described in type VI but described in other OFDS subtypes and similar syndromes. Our patient represents a transitional OFDS type, further supporting evidence of a common molecular pathway among these disorders. 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This report highlights the importance of the radiologist’s role in diagnosis.</description><subject>Case Report</subject><subject>Female</subject><subject>Humans</subject><subject>Imaging</subject><subject>Infant, Newborn</subject><subject>Larynx - abnormalities</subject><subject>Magnetic Resonance Imaging</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Neuroradiology</subject><subject>Nuclear Medicine</subject><subject>Oncology</subject><subject>Orofaciodigital Syndromes - diagnosis</subject><subject>Pediatrics</subject><subject>Radiology</subject><subject>Trachea - abnormalities</subject><subject>Ultrasound</subject><issn>0301-0449</issn><issn>1432-1998</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNqFkc-K1TAUxoM4ONfRB3AjwYXoInqSpk3iTgb_DFzQhc42pG0yk6FtapKL9AF8EJ9lXmxSemFAGNzkcMjv-w7nfAi9oPCOAoj3CYBxQQAkASkEWR6hHeUVI1Qp-RjtoAJKgHN1ip6mdAMAVU2rJ-iUSi4kY2yH_uxNXKYrawZsph7naLrrrQmjGbxN2E-lKa8zU8a_fb7GIZqBONP5Unp_5XPh0zL1MYwW52W2-PICv7m8_RtN78l3M89vP-Bo5xAzDg6bdcqUfPZhKspV8AydODMk-_xYz9DPz59-nH8l-29fLs4_7knHATLhrlWtZb2gStSmcY7WRlHglDtVd7arjGq7toHaSFE7qdq6aXjDJAiraM3a6gy93nznGH4dbMp69Kmzw2AmGw5JN6oSIEH-F2QgZbnmCr76B7wJh1j2KgxjjWJM8gLRDepiSClap-fox3J4TUGvSeotSV2S1GuSeimal0fjQzva_l5xjK4AbANS-SoJxvvJD7veAbvFqjU</recordid><startdate>20080901</startdate><enddate>20080901</enddate><creator>Hayes, Laura L.</creator><creator>Simoneaux, Stephen F.</creator><creator>Palasis, Susan</creator><creator>Niyazov, Dmitriy M.</creator><general>Springer-Verlag</general><general>Springer Nature B.V</general><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>3V.</scope><scope>7QP</scope><scope>7RV</scope><scope>7TK</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7T2</scope><scope>7U2</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>20080901</creationdate><title>Laryngeal and tracheal anomalies in an infant with oral-facial-digital syndrome type VI (Váradi-Papp): report of a transitional type</title><author>Hayes, Laura L. ; Simoneaux, Stephen F. ; Palasis, Susan ; Niyazov, Dmitriy M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c400t-4fb9be2d71975a6ff15a910414f95cec3a9bcb605a875f89b566462807e9152b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Case Report</topic><topic>Female</topic><topic>Humans</topic><topic>Imaging</topic><topic>Infant, Newborn</topic><topic>Larynx - 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There are 13 subtypes of the OFDS, and much overlap exists among OFDS patients. Distinct syndromes such as Joubert and Pallister-Hall display many of the same features. This report describes an infant with abnormalities including a hypoplastic/absent cerebellar vermis and forked third metacarpals, consistent with a diagnosis of OFDS type VI (Váradi-Papp). The girl’s abnormalities also included malformations of the larynx and trachea, findings never before described in type VI but described in other OFDS subtypes and similar syndromes. Our patient represents a transitional OFDS type, further supporting evidence of a common molecular pathway among these disorders. This report highlights the importance of the radiologist’s role in diagnosis.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer-Verlag</pub><pmid>18478222</pmid><doi>10.1007/s00247-008-0877-y</doi><tpages>5</tpages></addata></record> |
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subjects | Case Report Female Humans Imaging Infant, Newborn Larynx - abnormalities Magnetic Resonance Imaging Medicine Medicine & Public Health Neuroradiology Nuclear Medicine Oncology Orofaciodigital Syndromes - diagnosis Pediatrics Radiology Trachea - abnormalities Ultrasound |
title | Laryngeal and tracheal anomalies in an infant with oral-facial-digital syndrome type VI (Váradi-Papp): report of a transitional type |
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