Hanhart's syndrome: clinical report on anatomofunctional aspects (2017)
- Authors:
- Autor USP: FUKUSHIRO, ANA PAULA - FOB
- Unidade: FOB
- Subjects: ANORMALIDADES CONGÊNITAS; INTERDISCIPLINARIDADE; QUALIDADE DE VIDA
- Language: Inglês
- Abstract: Introduction: Hanhart or Aglossia-adactyly is a rare congenital syndrome of unknownetiology that is characterized by deficient limb development with hypoplasia fingers,oligodactyly, syndactyly, micrognathia, incompletely developed tongue or even aglossia.Objective: To describe the case of an individual with diagnosis of Hanhart or Aglossia-adactyly syndrome regarding structural and functional disorders of the oral cavity. ClinicalReport: RNL, 6-years old, male, resident of Manaus-AM, history of maternal smoking,alcohol use, drug use and syphilis during pregnancy. Patient presented left forearm and leftlower limb phocomelia, syndactyly from the 2nd to 4th finger of the right hand, andmalformation on the right toes. Micrognathia, intact palate with adequate velum mobility,absence of deciduous teeth, presence of permanent 1st molar and congenital aglossia wereobserved on examination of the oral cavity. By means of videofluoroscopy swallowing study,oropharyngeal dysphagia was observed, with great impairment to the oral phase, laryngealpenetration during opening of the pharyngoesophageal transition, residue in vallecula andpyriform sinus with cleaning after multiple swallows. A head compensation and laryngealelevation movement were spontaneously used by the patient. Conclusion: Understandingthat the syndrome is rare, and that the individual in the study has comorbidities associatedwith Hanhart syndrome, an interdisciplinary follow-up is required in order to minimizephysical, functional and social impacts of the related symptoms and, consequently, toprovide a better quality of life for the patient.
- Imprenta:
- Publisher: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo
- Publisher place: Bauru
- Date published: 2017
- Source:
- Título: Anais
- Conference titles: Simpósio Internacional de Fissuras Orofaciais e Anomalias Relacionadas
-
ABNT
ARAÚJO, Laryssa Lopes de et al. Hanhart's syndrome: clinical report on anatomofunctional aspects. 2017, Anais.. Bauru: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, 2017. Disponível em: https://repositorio.usp.br/directbitstream/5e3ba6b9-e72d-48b2-93e5-2d0c7143620f/2940281.pdf. Acesso em: 28 dez. 2025. -
APA
Araújo, L. L. de, Sá, Á. J. de A., Ferlin, F., & Fukushiro, A. P. (2017). Hanhart's syndrome: clinical report on anatomofunctional aspects. In Anais. Bauru: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/5e3ba6b9-e72d-48b2-93e5-2d0c7143620f/2940281.pdf -
NLM
Araújo LL de, Sá ÁJ de A, Ferlin F, Fukushiro AP. Hanhart's syndrome: clinical report on anatomofunctional aspects [Internet]. Anais. 2017 ;[citado 2025 dez. 28 ] Available from: https://repositorio.usp.br/directbitstream/5e3ba6b9-e72d-48b2-93e5-2d0c7143620f/2940281.pdf -
Vancouver
Araújo LL de, Sá ÁJ de A, Ferlin F, Fukushiro AP. Hanhart's syndrome: clinical report on anatomofunctional aspects [Internet]. Anais. 2017 ;[citado 2025 dez. 28 ] Available from: https://repositorio.usp.br/directbitstream/5e3ba6b9-e72d-48b2-93e5-2d0c7143620f/2940281.pdf - Análise perceptiva, nasométrica e aerodinâmica da fala de indivíduos submetidos à cirurgia de retalho faríngeo para a correção da insuficiência velofaríngea
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