Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Khalid Mohammed Al Attas"'
Autor:
Sultan Mohammad Bajawi, MD, Sultan Aqeel Jafarri, MD, Mohammed Ali Buraik, MD, Khalid Mohammed Al Attas, MD, Hasan Yehia Hannani, MD
Publikováno v:
JAAD Case Reports, Vol 4, Iss 3, Pp 232-234 (2018)
Externí odkaz:
https://doaj.org/article/6203d9aa9c414e3b8118e82a88a049da
Autor:
Mohammad Kamrul Ahsan, Khalid Mohammed Al Attas, Mohammed A. Buraik, Ali Mohammed Al-Sheikh, Sultan M. Bajawi
Publikováno v:
Journal of Dermatology and Dermatologic Surgery, Vol 21, Iss 2, Pp 81-83 (2017)
Chromoblastomycosis is a rare, chronic fungal infection of skin and subcutaneous tissue. It is caused by several pigmented fungi commonly seen in tropical and sub-tropical regions. Here, we report a case of chronic cutaneous chromoblastomycosis in a
Externí odkaz:
https://doaj.org/article/feb86b0518c847948b5c5789b12e4042
Autor:
AliMohammed Al-Sheikh, Khalid Mohammed Al Attas, Mohammed A. Buraik, Amr Mohammed Gamal, Mohammad Kamrul Ahsan
Publikováno v:
Journal of Dermatology and Dermatologic Surgery, Vol 20, Iss 2, Pp 139-141 (2016)
Interstitial granulomatous dermatitis (IGD) is an uncommon idiopathic dermatitis characterized by variable clinical presentation and a special histopathologic pattern. IGD is in some cases associated with autoimmune connective tissue diseases. Here w
Externí odkaz:
https://doaj.org/article/8fb960bdc7004889960754841bf4e869
Autor:
Khalid Mohammed Al Attas, Mohammad Kamrul Ahsan, Hasan Yehia Hannani, Amr Mohammed Gamal, Srinivas Bhavanarushi
Publikováno v:
Journal of Dermatology and Dermatologic Surgery, Vol 19, Iss 2, Pp 120-122 (2015)
Tuberculosis cutis orificialis (TCO) is a rare manifestation of cutaneous tuberculosis. Due to its variable clinical features, the diagnosis may be missed at the onset of the disease. Here we describe, TCO as well as intestinal tuberculosis in a pati
Externí odkaz:
https://doaj.org/article/7a763a3c29344f59b19dd47b52aef812
Autor:
Khalid Mohammed Al Attas, Mohammed A. Buraik, Hasan Yehia Hannani, Sultan M. Bajawi, Sultan Aqeel Jafarri
Publikováno v:
JAAD Case Reports
JAAD Case Reports, Vol 4, Iss 3, Pp 232-234 (2018)
JAAD Case Reports, Vol 4, Iss 3, Pp 232-234 (2018)
The first description of this condition in 1948 was followed by 17 case reports before Happle delineated the key features and proposed the acronym CHILD syndrome in 1980, which stands for congenital hemidysplasia, ichthyosiform nevus, and limb defect
Autor:
Ali Mohammed Al-Sheikh, Mohammed A. Buraik, Khalid Mohammed Al Attas, Mohammad Kamrul Ahsan, Sultan M. Bajawi
Publikováno v:
Journal of Dermatology and Dermatologic Surgery, Vol 21, Iss 2, Pp 81-83 (2017)
Chromoblastomycosis is a rare, chronic fungal infection of skin and subcutaneous tissue. It is caused by several pigmented fungi commonly seen in tropical and sub-tropical regions. Here, we report a case of chronic cutaneous chromoblastomycosis in a
Autor:
Khalid Mohammed Al-attas, Ali Hassan Najmi, Mosa Mohmmed Hassan Tawhari, Ibrahim Hassan Najmi, Mohammed Abdu Tawhari, Fawaz Tawhari, Khaled Ahamed Hassan Khbrani, Majed Hassan Mathkur, Khadija Hafed Sawadi
Publikováno v:
Clinics and Practice, Vol 8, Iss 4 (2018)
Clinics and Practice
Clinics and Practice
Actinomycosis is a subacute or chronic suppurative bacterial infection which caused because of filamentous gram-positive, anaerobic to microaerophilic nonacid fast bacilli primarily of the genus Actinomyces that normally colonize the mouth, colon, an
Autor:
Amr Mohamed Gamal, Sanjay Kumar, Khalid Mohammed Al Attas, Mohammad Kamrul Ahsan, Mohammed A. Buraik, Amr Abduljabbar
Publikováno v:
Journal of Dermatology and Dermatologic Surgery, Vol 19, Iss 1, Pp 47-50 (2015)
Juvenile xanthogranuloma (JXG) is a histiocytic disorder that is usually benign and limited to the skin. Usually it regresses spontaneously, more often without or with limited skin changes. The systemic form of JXG is rare and may be associated with
Autor:
Amr Mohammed Gamal, Khalid Mohammed Al Attas, AliMohammed Al-Sheikh, Mohammad Kamrul Ahsan, Mohammed A. Buraik
Publikováno v:
Journal of Dermatology and Dermatologic Surgery, Vol 20, Iss 2, Pp 139-141 (2016)
Interstitial granulomatous dermatitis (IGD) is an uncommon idiopathic dermatitis characterized by variable clinical presentation and a special histopathologic pattern. IGD is in some cases associated with autoimmune connective tissue diseases. Here w
Autor:
Mohammad Kamrul Ahsan, Hasan Yehia Hannani, Mohammed A. Buraik, Amr Mohamed Gamal, Khalid Mohammed Al Attas
Publikováno v:
Journal of the Saudi Society of Dermatology & Dermatologic Surgery. 17:69-72
Pyoderma gangrenosum is an inflammatory disease that has been found to be associated with many systemic illnesses. Here we describe, first time to our knowledge of pyoderma gangrenosum as well as pyostomatitis vegetans in a patient with hypogonadotro