Zobrazeno 1 - 10
of 405
pro vyhledávání: '"CUTIS marmorata telangiectatica congenita"'
Publikováno v:
Cirugía Pediátrica (English Edition). Jan2024, Vol. 37 Issue 1, p33-36. 4p.
Publikováno v:
Indian Journal of Paediatric Dermatology, Vol 25, Iss 3, Pp 237-239 (2024)
Cutis marmorata telangiectatica congenita (CMTC) is a rare capillary malformation characterized by persistent reticulated marbled erythema. A 16-year-old boy presented with reddish net-like lesion over the left side of his body which was initially no
Externí odkaz:
https://doaj.org/article/0dfaeb6c5c364a2cb0240882d5167ea9
Autor:
Serena Shah, Natasha Ferreira Santos da Cruz, Francisco Lopez-Font, Lauren Kiryakoza, Audina Berrocal
Publikováno v:
American Journal of Ophthalmology Case Reports, Vol 34, Iss , Pp 102067- (2024)
Purpose: To report 2 cases of enlarged foveal avascular zone (FAZ) on optical coherence angiography (OCTA) imaging in pediatric patients with cutis marmorata telangiectatica congenita (CMTC). Observations: A 10-week-old female and a 3-year-old male d
Externí odkaz:
https://doaj.org/article/e494f7bca9a34cffa67ee216279b7f2a
Autor:
Ben Lagha, Imene1 imenebenlagha@gmail.com, Zaara, Soumaya Youssef1, Harbaoui, Sarra1, Jaber, Kahena1, Dhaoui, Mohamed Raouf1, Doss, Nejib1
Publikováno v:
Our Dermatology Online / Nasza Dermatologia Online. Oct2018, p440-442. 3p.
Autor:
Deshpande, Ajay J.1 deshpandeajay.68@gmail.com
Publikováno v:
Journal of Cosmetic & Laser Therapy. Jun2018, Vol. 20 Issue 3, p145-147. 3p.
Publikováno v:
Diving & Hyperbaric Medicine: Journal of the South Pacific Underwater Medicine Society; Sep2023, Vol. 53 Issue 3, p285-289, 5p
Publikováno v:
Indian Journal of Paediatric Dermatology. Jul-Sep2016, Vol. 17 Issue 3, p215-217. 3p.
Autor:
Kienast, A. K.1, Hoeger, P. H.1 hoeger@kkh-wilhelmstift.de
Publikováno v:
Clinical & Experimental Dermatology. Apr2009, Vol. 34 Issue 3, p319-323. 5p. 3 Charts.
Autor:
Villa, Antonio antonio_villa@fastwebnet.it, Fiocchi, Mara
Publikováno v:
Emergency Care Journal. 2020, Vol. 16 Issue 3, p158-159. 2p.
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
Rubinstein-Taybi syndrome (RSTS) is a rare autosomal dominantly inherited disease characterized by slow mental and physical growth, skeletal abnormalities (broad thumbs and big toes), and dysmorphic facial features. RSTS is associated with de novo va
Externí odkaz:
https://doaj.org/article/c62a05dc5d2544679f2dcd8852d4ce6a