Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Hypodactylia"'
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
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:
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),
Autor:
Ipek Guney Varal, Pelin Dogan
Publikováno v:
The Pan African Medical Journal
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
Autor:
Harold Chen
Publikováno v:
Atlas of Genetic Diagnosis and Counseling ISBN: 9781461464303
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a81574ed3bf38bd1d13286845258520b
https://doi.org/10.1007/978-1-4939-2401-1_126
https://doi.org/10.1007/978-1-4939-2401-1_126
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 74:1092-1094
Hypoglossia is a rare congenital anomaly and is frequently associated with limb anomalies. In 1971, Hall employed the term hypoglossia-hypodactylia syndrome for the classification of these oromandibular-limb hypogenesis syndromes. The syndrome is cha
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
Publikováno v:
岐阜歯科学会雑誌 = The Journal of Gifu Dental Society. 32(2-3):1-5
顎顔面形態について、CT・MRIを用いた三次元画像解析を行うことは、 1)従来のエックス線写真などの二次元投影画像では重なって表示される構造物の位置関係を三次元的に把握できるこ
Publikováno v:
The Cleft Palate-Craniofacial Journal. 40:196-202
Objective To present the morphology of the extremities, craniofacial structures, and the oral cavity based on roentgencephalometry and three-dimensional computed tomography and magnetic resonance imaging scanning in a patient with hypoglossia-hypodac