Zobrazeno 1 - 10 of 25 pro vyhledávání: '"Hallermann Streiff Francois Syndrome"'
1
Combined orthodontic and surgical treatment for a patient with Hallermann-Streiff-Francois syndrome, severe obstructive sleep apnea, and history of antiresorptive medication
Autor: Stanimira I. Kalaykova, Frank Baan, Caroline F.W. Sondeijker, Johanna K.M. Maertens, Ruben C. Apperloo
Publikováno v: American Journal of Orthodontics and Dentofacial Orthopedics, 159, 97-107
American Journal of Orthodontics and Dentofacial Orthopedics, 159, 1, pp. 97-107
Micrognathia and retrognathia, as observed in patients with the Hallermann-Streiff-Francois syndrome, might result in obstructive sleep apnea syndrome. When it becomes severe (apnea-hypopnea index [AHI], ≥30), noninvasive treatment options might be
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31f4af21b8ae07497283bb21127e3528
http://hdl.handle.net/2066/230143
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2
A familial study of Hallermann–Streiff–François syndrome
Autor: Côme Ebana Mvogo, C Bengondo, D Beleho, AT Bitang, VA Njami, E Epée
Publikováno v: International Medical Case Reports Journal.
E Epée,1 D Beleho,2 AT Bitang,3 VA Njami,4 C Bengondo,5 Côme Ebana Mvogo1 1Ophthalmology Department, Yaoundé University Teaching Hospital, Yaoundé, Cameroon; 2Ophthalmology Department, Okola District Hospital, Okola, Cameroon; 3Faculty of Medicin
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b775a7242304cdc1728812dcf64635b7
https://www.dovepress.com/a-familial-study-of-hallermann-streiff-francois-syndrome-peer-reviewed-article-IMCRJ
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3
Ophthalmologic manifestations of Hallermann-Streiff-Francois syndrome: report of four cases
Autor: Ramesh Kekunnaya, Teena Mariet Mendonca, Virender Sachdeva, B Pasyanthi
Publikováno v: Eye (London, England). 30(9)
PurposeHallermann-Streiff-Francois syndrome (HSS) is a rare genetic disorder characterised by ocular and craniofacial anomalies. The purpose of this report is to highlight the ophthalmological features in four such patients and outcomes of cataract s
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a95969e36acb79d6b31b42d96e0cec5
https://pubmed.ncbi.nlm.nih.gov/27472202
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4
MCA/MR syndrome with features of Hallermann-Streiff syndrome and 4q deficiency/ 14q duplication
Autor: F. Lemmens, H. Van Dern Berghe, Martine Borghgraef, J. P. Fryns
Publikováno v: Clinical Genetics. 44:146-148
In this report we present the clinical history and findings in a female newborn with 4q deficiency/14q duplication, the unbalanced product of a paternal t(4;14)(q33;q32). The clinical symptoms and signs observed in this child up to the age of 14 mont
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1cb8f3ec9eb4c6e0136ed81a1c635521
https://doi.org/10.1111/j.1399-0004.1993.tb03866.x
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5
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8
Hallermann-Streiff syndrome: a case review
Autor: F. Safar, A. Mirshekari
Publikováno v: Clinical and experimental dermatology. 29(5)
Hallermann-Streiff Syndrome is a rare genetic disorder that is characterized primarily by head and face abnormalities. Patients show bird-like facies, dental abnormalities, and hypotrichosis with various ophthalmic abnormalities. We report here a 26-
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4811f5d3b3fde8f7d0f643f18a37f819
https://pubmed.ncbi.nlm.nih.gov/15347328
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