Zobrazeno 1 - 10
of 272
pro vyhledávání: '"Oligodactyly"'
Autor:
Yaa Achiaa Afreh, FWACS, MBChB, BSc, Kwasi Adjepong Twum, FWACS, MGCP, MBChB, BSc, Adu Tutu Amankwa, FWACS, MBChB, BSc, Kwasi Ankomah, FGCP, MBChB, BSc, Obed Kojo Otoo, FGCP, MBChB, BSc, Caroline Oku, MGCP, MBChB, BSc
Publikováno v:
Radiology Case Reports, Vol 19, Iss 6, Pp 2211-2213 (2024)
Hemimelia denotes the partial or complete absence of the distal half of a limb. Ulna hemimelia, a rare congenital anomaly, involves the complete or partial absence of the ulna in the upper limb, with an incidence of 1 in 150,000. This condition has b
Externí odkaz:
https://doaj.org/article/39c009e997a24e958864bbcf8d7b9ce9
Akademický článek
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Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Sulaeman Sulaeman
Publikováno v:
Jurnal Aspikom, Vol 3, Iss 4, Pp 662-674 (2018)
The purpose of this research it is analyzing the management of the impression in the stage before it or the stage back displayed in the process of communication at the daily life of social interaction with the surrounding environment for people with
Externí odkaz:
https://doaj.org/article/71b135e8a3a147008df2af6c0a81fb8b
Publikováno v:
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-5 (2017)
Abstract Background Diagnostic Exome Sequencing (DES) has been shown to be an effective tool for diagnosis individuals with suspected genetic conditions. Case Presentation We report a male infant born with multiple anomalies including bilateral dyspl
Externí odkaz:
https://doaj.org/article/3b4a8130ebde489a9e0710d09cf2e8ab
Publikováno v:
LONTAR: Jurnal Ilmu Komunikasi; Vol. 10 No. 1 (2022): Lontar : Jurnal Ilmu Komunikasi; 25-32
People with oligodactyly are humans who have less than five fingers and toes. This deficiency is formed since their birth. This study involved five informants from Ulutaue Hamlet, Bone Regency of South Sulawesi Province, Indonesia. People with oligod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8029d8dd27c80d2a2371f40875855c02
https://e-jurnal.lppmunsera.org/index.php/LONTAR/article/view/3693
https://e-jurnal.lppmunsera.org/index.php/LONTAR/article/view/3693
Autor:
Masakuni Tagaki
Publikováno v:
Integrative Psychological and Behavioral Science. 55:486-496
In this commentary, I discuss the contribution of the target article (Sulaeman et al. 2020) and suggest further study in terms of research on psychosocial issues of people with physical disabilities. The authors of the target article qualitatively an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47a88b4c9d13a8db24bac5806a54e12f
https://doi.org/10.1007/s12124-020-09597-2
https://doi.org/10.1007/s12124-020-09597-2
Autor:
Sajid Malik, Muhammad Afzal
Publikováno v:
Journal of Research in Medical Sciences, Vol 18, Iss 9, Pp 818-821 (2013)
Ulnar hypoplasia is a rare longitudinal limb deficiency in which the ulna shows various degrees of deficiency. The condition is normally associated with radial defects, and in severe cases there is a reduction of postaxial/ulnar digits. Ulnar deficie
Externí odkaz:
https://doaj.org/article/f886f22b5c154252bf20673592868aeb
Autor:
Leyla Bulut, Cihat Aydogan, Samet Benli, Erdal Taskin, Mustafa Aydin, Talha Atasci, Berivan Karatas
Publikováno v:
Pediatric Oncall. 19
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85391086801cca904ffec14db4652a4a
https://doi.org/10.7199/ped.oncall.2022.3
https://doi.org/10.7199/ped.oncall.2022.3
Publikováno v:
Journal of Fetal Medicine. :159-164
Proximal femoral focal deficiency (PFFD) is a rare skeletal dysplasia, characterized by hypoplasia of the subtrochanteric femur with variable degrees of shortening of the femoral shaft. There are numerous gene e.g. TBX4, FGF, FGFR, TP63 and HOX respo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8a64a582a78cda2e3fdbda0356c9124
https://doi.org/10.1007/s40556-019-00213-x
https://doi.org/10.1007/s40556-019-00213-x