Zobrazeno 1 - 10
of 140
pro vyhledávání: '"Hypoglossia"'
Publikováno v:
Journal of Oral Medicine and Oral Surgery, Vol 28, Iss 2, p 17 (2022)
Background: A positive prenatal history of maternal fever has been found to express as a range of defects in infants including limb reduction, central nervous system defects, facial dysmorphogenesis and foetal death. Oromandibular limb hypogenesis sy
Externí odkaz:
https://doaj.org/article/38219c196f764963a594c5abc1897566
Autor:
Ipek Guney Varal, Pelin Dogan
Publikováno v:
The Pan African Medical Journal, Vol 32, Iss 213 (2019)
Hanhart syndrome is a congenital disorder that causes an undeveloped tongue and malformed extremities and fingers. Small mouth, short or incompletely developed tongue (hypoglossia), absent or shortened fingers and/or toes, jaw abnormalities such as m
Externí odkaz:
https://doaj.org/article/173d095930ef426ca6f9b3fcc900322c
Akademický článek
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Publikováno v:
Journal of Craniofacial Surgery. 31:e84-e89
Agnathia-otocephaly complex (AOC) is a rare malformation complex of the first pharyngeal arch that is characterized by agnathia/dysgnathia, microstomia, aglossia/hypoglossia and variable displacement of the ears. Only 11 post-infancy patients with se
Publikováno v:
The Journal of Craniofacial Surgery
Oromandibular limb hypogenesis syndrome is a rare developmental anomaly and only a few cases are reported with complete surgical and orthodontic rehabilitation. An adult male patient with isolated hypoglossia, micrognathism, hypodontia, (oromandibula
Hypoglossia Type 1A: Report of a case and review of literature with focus on clinical investigations
Publikováno v:
Indian Journal of Dental Research, Vol 23, Iss 2, Pp 264-270 (2012)
Hypoglossia is a rare entity which is reported sporadically. Hypoglossia has often occurred in an association with limb anomalies and, therefore, these cases have been grouped together as hypoglossia-hypodactylia within oromandibular limb hypogenesis
Externí odkaz:
https://doaj.org/article/a0037120fee24e658b7773a2d850a883
Publikováno v:
Journal of Dental Research, Dental Clinics, Dental Prospects, Vol 4, Iss 4, Pp 136-139 (2010)
The oromandibular-limb hypogenesis syndrome comprises a group of anomalies which simultaneously affect the mandible, tongue, and maxilla with or without reductive limb anomalies. It is characterized by failure of development of the intraoral region
Externí odkaz:
https://doaj.org/article/cdd06c993b124a70a788d5473f542ba0
Publikováno v:
Russian Journal of Pediatric Surgery. 23:206-210
Introduction. Aglossia / hypoglossia is a rare condition combined with underdeveled lower jaw, lack of mandibular incisors and various degrees of limb anomalies. In domestic and foreign literature, one can find only few such observations in pediatric
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 8, Iss 4, Pp SD01-SD02 (2014)
The Oromandibular Limb Hypogenesis Syndromes (OLHS) comprises a spectrum of disorders involving the tongue, mandible, and the limbs and are characterized by hypoplastic mandible, absence of the lower incisors, hypoglossia, digits and limbs abnormali
Externí odkaz:
https://doaj.org/article/10251403d1d84800ba97a6970a9336f7
Publikováno v:
Indian Journal of Case Reports. 5:53-55
Hanhart 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),