Zobrazeno 1 - 10
of 17
pro vyhledávání: '"hypopigmented skin lesions"'
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 14, Iss 2, Pp OD14-OD16 (2020)
Tuberous sclerosis is a rare autosomal dominant genetic disorder caused by mutation of TCS1 or TCS2 gene. The birth incidence is estimated to be 1 in 6000. It is a multisystem neurocutaneous disorder characterised by widespread hamartomas, cutaneous
Externí odkaz:
https://doaj.org/article/a215f699849d445fab0324bfbbf25371
Publikováno v:
Pediatric dermatologyREFERENCES. 37(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6cd8b4c54e677e37b6755a9f05a61ed
https://pubmed.ncbi.nlm.nih.gov/31997459
https://pubmed.ncbi.nlm.nih.gov/31997459
A case of hypomelanosis of Ito accompanied by unilateral abnormal limb overgrowth and delayed speech
Publikováno v:
Northern Clinics of Istanbul
İstanbul Kuzey Klinikleri, Vol 7, Iss 1, Pp 71-73 (2020)
İstanbul Kuzey Klinikleri, Vol 7, Iss 1, Pp 71-73 (2020)
Hypomelanosis of Ito (HI) is characterized by unilateral or bilateral hypopigmented skin lesions and usually presents as a multisystemic disorder. Skin lesions may develop in different textures, such as linear, whorled, or patchy, and are often accom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17f2732897a478e389a3900246701452
http://europepmc.org/articles/PMC7103738
http://europepmc.org/articles/PMC7103738
Autor:
Subhash Dasarathan, Avijit Mondal
Publikováno v:
Clinical Cases in Disorders of Melanocytes ISBN: 9783030227562
Leprosy (Hansen’s disease) is a chronic infectious disease caused by Mycobacterium leprae, primarily affecting the peripheral nerves, and skin. In persons with high bacillary load (lepromatous pole), the internal organs also may be affected. A 19-y
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00eaa8e825b4f924d9e47f40c38f5b3e
https://doi.org/10.1007/978-3-030-22757-9_19
https://doi.org/10.1007/978-3-030-22757-9_19
Publikováno v:
American Journal of Medical Genetics Part A. 164:2947-2951
Oculoectodermal syndrome (OMIM 600268) is rare and characterized by aplasia cutis congenita, epibulbar dermoids, and other abnormalities. We report herein on a newly recognized patient with oculoectodermal syndrome, which is the 19th reported patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f837e30376e401d719ef6b3fef72d0ee
https://doi.org/10.1002/ajmg.a.36727
https://doi.org/10.1002/ajmg.a.36727
Autor:
Bharath A Chhabria, Neelam Varma, Pulkit Rastogi, Subhash Varma, Sreejesh Sreedharanunni, Ashok Kumar Pannu
Publikováno v:
QJM : monthly journal of the Association of Physicians. 110(3)
A 29-year-old female had a history of hypopigmented skin lesions over the left cheek, back and thighs for over 3 years. These lesions were not associated with itching or any altered sensation but were progressively increasing in size and number. She
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aae0698431276c60d19c600bc24af4de
https://pubmed.ncbi.nlm.nih.gov/28011849
https://pubmed.ncbi.nlm.nih.gov/28011849
Autor:
Filipa Leite, Maria Miguel Gomes, Armando N. Pinto, Tereza Oliva, Cláudia Patraquim, António Santos, Carla Garcez
Publikováno v:
Case Reports in Pediatrics
Case Reports in Pediatrics, Vol 2016 (2016)
Case Reports in Pediatrics, Vol 2016 (2016)
Primary cutaneous lymphomas (PCL) are rare in pediatrics. Mycosis fungoides (MF) is the most frequent PCL diagnosed in childhood. There are various clinical variants of MF, including the hypopigmented MF (HMF). We present a 5-year-old boy with an 18-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31619a7c2c5ad2ac0c3e6bc55f35bb5c
http://europepmc.org/articles/PMC5153468
http://europepmc.org/articles/PMC5153468
Publikováno v:
Skin Research and Technology. 12:298-302
Background/purpose: Vitiligo and nevus depigmentosus (ND) present similar hypopigmented macules with significantly different prognoses. Although the distinction between the two diseases is important, differential diagnosis relies on medical history a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86e981ad3bf4855bd317f050e8061599
https://doi.org/10.1111/j.0909-752x.2006.00187.x
https://doi.org/10.1111/j.0909-752x.2006.00187.x
Publikováno v:
Pediatric dermatology. 31(6)
The prevalence of celiac disease (CD) is increasing and may be as high as 1% of the US population. The typical presentation of CD generally includes gastrointestinal symptoms, but more individuals are presenting with extraintestinal manifestations. A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa8cc9e0ff9539ab6aacca6c35466df1
https://pubmed.ncbi.nlm.nih.gov/25382799
https://pubmed.ncbi.nlm.nih.gov/25382799
Autor:
Emmanuel Mahé, Y. De Prost, B. Flageul, P. Buffet, Sylvie Fraitag, K. Marrou, Smail Hadj-Rabia
Publikováno v:
Archives de Pédiatrie. 12:1145-1147
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::04bbe1e4f3008adb7ae7460580699fda
https://doi.org/10.1016/j.arcped.2005.03.056
https://doi.org/10.1016/j.arcped.2005.03.056