Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Sultan Al-Khenaizan"'
Autor:
Alfred Ammoury, Ahmed Ameen, Mahira Hamdy El Sayed, Sultan Al-Khenaizan, Nehal Hassan, Marcelle Ghoubar
Publikováno v:
Dermatology and Therapy, Vol 13, Iss 3, Pp 769-785 (2023)
Abstract Introduction Atopic dermatitis (AD) is a complex inflammatory disease of the skin that has a significant impact on the well-being of patients and their families. The prevalence of AD has increased in developing countries and regions, includi
Externí odkaz:
https://doaj.org/article/31726b2dd3af4072b326edb14d4f3237
Publikováno v:
JAAD Case Reports, Vol 39, Iss , Pp 53-54 (2023)
Externí odkaz:
https://doaj.org/article/a8dc40615f4d4ad3bc8f2f4702cdb923
Publikováno v:
Case Reports in Dermatology, Vol 13, Iss 3, Pp 470-473 (2021)
Ichthyosis prematurity syndrome is a rare autosomal recessive genodermatosis that is associated with mutations in the SLC27A4 gene. Its onset occurs in early childhood and presents with the clinical triad of premature birth, thick caseous desquamatin
Externí odkaz:
https://doaj.org/article/9ff3d4d350394a72882c36d0c6906300
Autor:
Khalid Al Hawsawi, Mazin Al Jabri, Mazen S. Dajam, Bashaer Almahdi, Waseem K. Alhawsawi, Safdar Abbas, Abeer Al Tuwaijri, Muhammad Umair, Majid Alfadhel, Sultan Al-Khenaizan
Publikováno v:
Frontiers in Genetics, Vol 13 (2022)
Background: Hypotrichosis with Recurrent Skin Vesicles (HYPTSV) is an extremely rare condition, having autosomal recessive inheritance. Here in we report a 4-years- old Saudi boy who presented with a history of recurrent skin blisters that are locali
Externí odkaz:
https://doaj.org/article/b8bed27256b247d09faac4193028f4c5
Autor:
Raghad Alharthi, Muhannad A. Alnahdi, Ahad Alharthi, Seba Almutairi, Sultan Al-Khenaizan, Mohammed A. AlBalwi
Publikováno v:
Frontiers in Genetics, Vol 12 (2022)
Epidermolysis bullosa (EB) is a rare heterogeneous genetic mechanobullous skin disorder that is characterized by increased skin fragility leading to blistering following minor trauma. EB may be inherited as an autosomal dominant or an autosomal reces
Externí odkaz:
https://doaj.org/article/5ce8dd4ea16146fbbc9a2e1a7df5b1b8
Autor:
Huda Al-Rwebah, MBBS, Rayan Alkhodair, MBBS, FRCPC, FAAD, Sultan Al-Khenaizan, MBBS, FRCPC, DABD
Publikováno v:
JAAD Case Reports, Vol 6, Iss 4, Pp 359-361 (2020)
Externí odkaz:
https://doaj.org/article/fbd6c25abb534bd88cfbbee910738b01
Publikováno v:
Journal of Dermatology and Dermatologic Surgery, Vol 24, Iss 1, Pp 51-51 (2020)
Subcision using a Nokor needle is commonly performed to treat acne scars. We describe a new method to maintain proper needle orientation during subcision.
Externí odkaz:
https://doaj.org/article/a94e65da88cf4c689e31bfa89720d71e
Publikováno v:
Case Reports in Dermatology, Vol 13, Iss 3, Pp 470-473 (2021)
Case Reports in Dermatology
Case Reports in Dermatology
Ichthyosis prematurity syndrome is a rare autosomal recessive genodermatosis that is associated with mutations in the SLC27A4 gene. Its onset occurs in early childhood and presents with the clinical triad of premature birth, thick caseous desquamatin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7431cd6c105201202c255026de57ce8a
https://www.karger.com/Article/FullText/519035
https://www.karger.com/Article/FullText/519035
Autor:
Sultan Al-Khenaizan, Luluah Al-Mubarak
Publikováno v:
Saudi Medical Journal. 42:454-456
Clinical Presentation A 2-month-old baby boy, of full-term spontaneous vaginal delivery, presented to the dermatology outpatient clinic with generalized erythroderma, which had been noted since birth. Family history was positive for similar disease i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c64a533afd02a3d03d43d1355d7f5d5
https://doi.org/10.15537/smj.2021.42.4.20200757
https://doi.org/10.15537/smj.2021.42.4.20200757
Publikováno v:
JAAD Case Reports
JAAD Case Reports, Vol 6, Iss 4, Pp 359-361 (2020)
JAAD Case Reports, Vol 6, Iss 4, Pp 359-361 (2020)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6962e9b58e93c6e2ca522aae2e5d2348
https://doi.org/10.1016/j.jdcr.2020.01.028
https://doi.org/10.1016/j.jdcr.2020.01.028