Zobrazeno 1 - 10
of 257
pro vyhledávání: '"Hallermann–Streiff syndrome"'
Autor:
Frontiers Production Office
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
Externí odkaz:
https://doaj.org/article/a758e9d4d512438f8e1d998f0f74ca2b
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Hallermann-Streiff syndrome (HSS) is a rare congenital syndrome with different anomalies including midface hypoplasia, beak nose and micrognathia. The upper airways narrowness can lead to severe respiratory complications such as obstructive sleep apn
Externí odkaz:
https://doaj.org/article/a88c8d3f39474d57ae157b03a395fe97
Autor:
Nour Ammar, Magda M. El-Tekeya
Publikováno v:
Frontiers in Dental Medicine, Vol 3 (2022)
Hallermann–Streiff syndrome (HSS) is a disorder of rare occurrence affecting the craniofacial complex, with approximately 200 cases reported in the literature. Nonetheless, its distinctive facial features render it highly recognizable. We present t
Externí odkaz:
https://doaj.org/article/25fd6da1a1774331bdd3eebe8b770f85
Publikováno v:
Journal of Limb Lengthening & Reconstruction, Vol 5, Iss 1, Pp 47-50 (2019)
Hallermann–Streiff syndrome (HSS) is a relatively rare genetic disorder causing mainly dysmorphic craniofacial features. Very few cases are reported in the literature, none of which reported lower limb skeletal deformity. The main objective of this
Externí odkaz:
https://doaj.org/article/26d6a3284ca345748c91e5c9f9037bee
Publikováno v:
Journal of Stomatology, Oral and Maxillofacial Surgery. 123:e219-e223
Hallermann Streiff Syndrome (HSS) is a rare congenital abnormality with about 200 case reports in the literature. Its etiology is unknown although it may be due to a sporadic mutation. Diagnosis is based on the association of craniofacial malformatio
Autor:
S Rashmi, Praveen S Alavandi
Publikováno v:
Archives of Medicine and Health Sciences, Vol 5, Iss 2, Pp 242-244 (2017)
Hallermann–Streiff syndrome (HSS) is a rare congenital disorder with multiple abnormalities mainly affecting face, skull, hair, eyes, and teeth. We report a case of an 18-year-old Indian girl with HSS having typical physical features and ophthalmol
Externí odkaz:
https://doaj.org/article/cbbdf1497edf4da59a8c32af8dad69b0
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Rabolu Elena
Publikováno v:
Sport şi Societate, Vol 15, Iss Special, Pp 197-205 (2015)
The purpose of this paper is to underline once again kinesitherapy’s role and importance in the recovery of children with serious motor, neuro-vegetative and joint disorders induced by chromosomal modifications. The actual research consisted of a s
Externí odkaz:
https://doaj.org/article/5a85e91d00804552a85f643a14b82832
Publikováno v:
Journal of Craniofacial Surgery. 32:e20-e23
Hallermann-Streiff syndrome is a rare congenital abnormality involving multiple craniofacial malformations, such as micrognathia, prominent frontal and nasal bones, vision defects, and dental anomalies. In most patients, patients affected with this d
Publikováno v:
Journal of Indian Academy of Oral Medicine and Radiology, Vol 23, Iss 3, Pp 237-240 (2011)
The Hallermann-Streiff syndrome (HSS) is a rare congenital disorder characterized by distinctive craniofacial malformations and significant orodental abnormalities. A relative lack of dental literature regarding this syndrome has been noted. Most cas
Externí odkaz:
https://doaj.org/article/2e5d483f6421485faa87593cf8794b55