Hanhart Syndrome: A Rare Case Report And Review Of Literature

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dc.contributor.authorDas, Shreyaen_US
dc.contributor.authorMazumdar, Anjanaen_US
dc.contributor.authorMaity, Bikash Chandraen_US
dc.contributor.authorGhose, Sandipen_US
dc.date.accessioned2020-01-02T06:31:25Z
dc.date.available2020-01-02T06:31:25Z
dc.date.issued2019-01
dc.description.abstractHanhart syndrome is a rare congenital and genetic disease, in which the most common signs are short, incompletely developed tongue (hypoglossia), absent or partially missing fingers and/or toes (hypodactylia), malformed arms and/or legs (peromelia), and small jaw (micrognathia). Here, we report a case of Hanhart syndrome in an 18-year-old boy. The boy presented with few extraoral and intraoral abnormalities such as short toes and phalanges along with partial syndactyly in the left hand only were the most relevant. Other features such as micro and retrognathic face, incompetent lips, and wide nasal bridge were also significant. The boy was suffering for difficulties in speech and swallowing due to small tongue size, high arched palate, crowding, and few missing teeth. To provide adequate treatment to a patient with Hanhart syndrome, this study aimed to review and to analyze this literature and treatment protocols.en_US
dc.identifier.affiliationsPG Student, Dr. R. Ahmed Dental College and Hospital, Kolkata, West Bengal, Indiaen_US
dc.identifier.affiliationsProfessor and Head, Dr. R. Ahmed Dental College and Hospital, Kolkata, West Bengal, Indiaen_US
dc.identifier.affiliationsDepartment of Oral Pathology, Dr. R. Ahmed Dental College and Hospital, Kolkata, West Bengal, Indiaen_US
dc.identifier.affiliationsAssistant professor, Dr. R. Ahmed Dental College and Hospital, Kolkata, West Bengal, Indiaen_US
dc.identifier.citationDas Shreya, Mazumdar Anjana, Maity Bikash Chandra, Ghose Sandip. Hanhart Syndrome: A Rare Case Report And Review Of Literature. Indian Journal of Case Reports. 2019 Jan; 5(1): 53-55en_US
dc.identifier.issn2454-129X
dc.identifier.issn2454-1303
dc.identifier.placeIndiaen_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/190800
dc.languageenen_US
dc.publisherAtharva Scientific Publicationsen_US
dc.relation.issuenumber1en_US
dc.relation.volume5en_US
dc.source.urihttps://doi.org/10.32677/IJCR.2019.v05.i01.018en_US
dc.titleHanhart Syndrome: A Rare Case Report And Review Of Literatureen_US
dc.typeJournal Articleen_US
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