Search Results - "Sleiay, Mouhammed"

Hyperglycemia with hypogonadism and growth hormone deficiency in a 17-year-old male with H syndrome: the first case report from Syria by Hamsho, Suaad, Alaswad, Mohammed, Sleiay, Mouhammed, Alhusseini, Ayham

“…The nucleoside transport capabilities of the human equilibrative nucleoside transporter-3 (hENT3) are disrupted by mutations in SLC29A3 (10q22.2), which are…”
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Pauci‐immune necrotizing glomerulonephritis in a 24‐year‐old female with negative ANCA antibodies: A rare case report by Hamsho, Suaad, Dumirieh, Sumaya, Sleiay, Mouhammed, AlBaroudi, Douha, Alshekh, Muhamad Ali, Alahmad, Marwa

“…Key Clinical Message Pauci‐immune necrotizing glomerulonephritis (PING) is a small vessel renal vasculitis usually associated with the presence of…”
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A 23‐year‐old patient with bilateral hypoplastic thumbs and toes: A case report by Hamsho, Suaad, Sleiay, Mouhammed, Alaswad, Mohammed, Alsmodi, Hasan, Al‐Hakeem, Khaled

“…Key Clinical Message However, it is noteworthy that certain patients with minor functional limitations in their hand may have experienced undiagnosed thumb…”
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Uremic encephalopathy manifesting with a unique MRI finding (the lentiform fork sign) in an adult male: A case report by Alhusseini, Ayham, Hamsho, Suaad, Alabdullah, Hadi, Alaswad, Mohammed, Sleiay, Mouhammed, Alsamarrai, Omar

“…Key Clinical Message A novel radiologic sign in patients with renal failure and uremic encephalopathy (UE) with metabolic acidosis has recently been identified…”
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Lower urinary tract symptoms caused by scabies mites (sarcoptes scabiei): A case report by Alabdullah, Hadi, Alabdullah, Muhammad Nour, Alabdullah, Salim, Allugamie, Gihad, Douri, Thaer, Sleiay, Mouhammed

“…Lower urinary tract symptoms (LUTS) are including an overactive bladder, voiding and storing urine. The causes of LUTS include infectious and inflammatory. In…”
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A 28-year-old patient with tuberous sclerosis associated with renal angiomyolipoma:A rare case report and literature review by Haydar, Hasan, Sleiay, Mouhammed, Alqreea, Mohammed, Almohamed, Ahmad, Alrajab, Doaa, alsaleh, Malak, Lutfi, Mohamad Yasin

“…Tuberous sclerosis complex (TSC) is a genetically inherited disorder distinguished by the development of numerous benign neoplasms across multiple organ…”
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A 24‐year‐old patient with testicular benign capillary hemangioma: A rare case report by Haydar, Hasan, Sleiay, Mouhammed, Marina, Sliman, Haydar, Abdulrahman, Alqreea, Mohammed, Alomar, Bauthaina, Lutfi, Mohamad Yasin, Youssef, Simon

“…Key Clinical Message The importance of urologists and pathologists being knowledgable about primary testicular hemangiomas and other benign adult testicular…”
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Is there any association between celiac disease, myelodysplastic symdrome and primary sclerosing cholangitis?: A rare case report by Hamsho, Suaad, Hariri, Moudar Al, sleiay, Bilal, alhussen, Abdul hadi daher, Sleiay, Mouhammed

“…Celiac disease (CD) is an autoimmune disease characterized by a specific serological and histological profile. Hematological findings are one of the most…”
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Small bowel obstruction in a 29‐year‐old male with congenital peritoneal bands: A rare case report from Syria by Sleiay, Mouhammed, Sleiay, Bilal, Albaroudi, Douha, Alsmoudi, Hasan, abshi, Mohammad ali, Alaswad, Mohammed, Sleiay, Abdulazez, Arabi, Osama

“…Key clinical Message This case highlights the significance of maintaining clinical suspicion for CPBs in adults presenting with SBO. Early surgical…”
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A 64‐year‐old male with primary diffuse renal large B‐cell non‐Hodgkin lymphoma: A rare case report by Haydar, Hasan, Sleiay, Mouhammed, Alabdullah, Hadi, Al‐alloush, Rouba, Al_alloush, Nour, Lutfi, Mohamad Yasin, Youssef, Simon, Hamsho, Suaad

“…Key Clinical Message In the context of lymphoma, it is of paramount importance to perform subsequent Positron Emission Tomography‐Computed Tomography (PET‐CT)…”
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A 37-year-old female with a carotid body tumor (paraganglioma): A rare case report from Syria by Sleiay, Mouhammed, Alsmoudi, Hasan, Alqreea, Mohammed, Marina, Sliman, Kanaan, Ahmad Mostafa, Aljammal, Makia Ali

“…This case study presents the clinical details of a 37-year-old woman who presented with an asymptomatic swelling in the right supraclavicular region,…”
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A 23-year-old male patient with Kimura's disease without renal transplantation: a rare case report from Syria by Alsmoudi, Hasan, Sleiay, Mouhammed, Almohamed, Ahmad, Hamsho, Suaad, Alhadla, Ahmad, Alqreea, Mohammed, Alakhras, Abdulkareem

“…Kimura's disease (KD) is a chronic, nonmalignant inflammatory disorder that primarily affects subcutaneous tissue. It is typically characterized by painless…”
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Brucella spondylodiscitis that affected both cervical and lumbar spines: a rare case report from Syria by Alhusseini, Ayham, Hamsho, Suaad, Sleiay, Mouhammed, Alsmoudi, Hasan, Frzat, Ayham, Alabdullah, Hadi, Tawashi, Yamama

“…Brucellosis, the most common microbial zoonotic disease in the world, is endemic in both industrialized and underdeveloped countries. Between 2 and 53% of…”
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A 30-year-old female with dermatomyositis without high elevation of muscle enzymes: a rare case report from Syria by Hamsho, Suaad, Sleiay, Bilal, Sleiay, Mouhammed, Batrash, Obeda, Alabdullah, Hadi, Aboud, Majed

“…Dermatomyositis (DM), sometimes referred to as inflammatory and degenerative changes in the skin and muscles, is a rare autoimmune disorder. DM is…”
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A 15-year-old male with Peutz-Jeghers syndrome: a rare case report from Syria by Sleiay, Mouhammed, Alqreea, Mohammed, Alqreea, Ihsan, Alhasan, Omar, Sleiay, Bilal, Kanaan, Ahmad Mostfa, Alabdullah, Hadi

“…In addition to extra gastrointestinal hamartomatous polyps, Peutz-Jeghers syndrome (PJS), a rare but well-known hereditary disorder, generates mucocutaneous…”
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Idiopathic granulomatous mastitis with extramammary manifestations: a case report by Hamsho, Suaad, Alaswad, Mohammed, Alsmodi, Hasan, Sleiay, Mouhammed, Hoha, Ghofran, Alcheikh, Salwa

“…Granulomatous mastitis is a rare inflammatory disorder of the breast, which can be either idiopathic or due to secondary etiology. This disease affects women…”
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A 4-month-old male with Raghib syndrome: a rare case report from Syria by Sleiay, Mouhammed, Sleiay, Bilal, Batrash, Obeda, Alabdullah, Hadi, Alsmoudi, Hasan, AlBaroudi, Douha, Almohamed, Ahmad, Ali Abshi, Mohammad, Takkem, Saleh

“…Raghib syndrome is a rare congenital complication consisting of the termination of the left superior vena cava (LSVC) in the left atrium, an unroofed coronary…”
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A 4-month-old male baby with an orf lesion on his nose: a rare case report by Sleiay, Mouhammed, Alqreea, Mohammed, Alabdullah, Hadi, Almohamed, Ahmad, Alsmoudi, Hasan, Al-Zahran, Mulham, Katth, Mouhammed Rabee, Sleiay, Bilal

“…Ecthyma contagiosum, sometimes referred to as human orf, is a zoonotic disease caused by the orf virus that is mostly acquired by coming into contact with…”
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A complex case of univentricular heart with multiple congenital malformations diagnosed in a newborn: a case report and literature review by Hossin, Huda, Sleiay, Mouhammed, Kouran, Joudi, Alsuliman, Raghad Mahmoud, Kojok, Mhd Anas, Alkhateb, Nour Mohamad Najeb, Ghanem, Suha Giselle, Mansour, Marah, Alsuliman, Tamim, Takkem, Saleh

“…Univentricular heart disease is a relatively rare condition that affects infants, with a prevalence ranging from 0.05 to 0.1 per 1000 live births. It is…”
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A 28-year-old patient with tuberous sclerosis associated with renal angiomyolipoma:A rare case report and literature review by Haydar, Hasan, Sleiay, Mouhammed, Alqreea, Mohammed, Almohamed, Ahmad, Alrajab, Doaa, Alsaleh, Malak, Lutfi, Mohamad Yasin

“…Tuberous sclerosis complex (TSC) is a genetically inherited disorder distinguished by the development of numerous benign neoplasms across multiple organ…”
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