Cargando…

Sarcoidosis: a delayed or missed diagnosis in children

Detalles Bibliográficos
Autores principales:	Al-Mayouf, Sulaiman M., Al-Sonbul, Abdullah, Al Jumaah, Suleiman, Al-Hemidan, Amal
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	King Faisal Specialist Hospital and Research Centre 2006
Materias:	Brief Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6074449/ https://www.ncbi.nlm.nih.gov/pubmed/16861861 http://dx.doi.org/10.5144/0256-4947.2006.220

Ejemplares similares

A retrospective review of autoinflammatory diseases in Saudi children at a rheumatology clinic
por: Alenazi, Abdullatif, et al.
Publicado: (2012)

The impact of antiphospholipid antibodies in children with lupus nephritis
por: Al-Mayouf, Sulaiman M., et al.
Publicado: (2015)

Successful treatment of severe gastrointestinal manifestations of Henoch–Schonlein Purpura and factor XIII deficiency using cryoprecipitate transfusion
por: Al Sonbul, Abdullah, et al.
Publicado: (2015)

Systemic lupus erythematosus following acute lymphocytic leukemia
por: Al Mayouf, Sulaiman M., et al.
Publicado: (2006)

Systemic lupus erythematosus in Saudi children: Long-term outcome
por: Al-Mayouf, Sulaiman M
Publicado: (2011)

Electrocardiographic disturbances in children with systemic lupus erythematosus
por: AlTwajery, Mohammed, et al.
Publicado: (2018)

Extensive intramuscular manifestation of sarcoidosis with initially missed diagnosis and delayed therapy: a case report
por: Meyer, Niklaus, et al.
Publicado: (2017)

Extensive ulcerations due to pyoderma gangrenosum in a child with juvenile systemic lupus erythematosus and C1q deficiency
por: Abanomi, Hind, et al.
Publicado: (2008)

Outcome of children with systemic rheumatic diseases admitted to pediatric intensive care unit: An experience of a tertiary hospital
por: Al-Mayouf, Sulaiman M, et al.
Publicado: (2019)

Coexistence of endocrinopathies in children with rheumatic diseases
por: Alhomaidah, Doha, et al.
Publicado: (2016)

Periodic fever, rash and arthropathy in a child
por: Al-Mayouf, Sulaiman M
Publicado: (2005)

Familial arthropathies
por: Al-Mayouf, Sulaiman
Publicado: (2014)

The value of renal ultrasound in children with a first episode of urinary tract infection
por: Alshamsan, Layla, et al.
Publicado: (2009)

Prevalence of fall injuries and risk factors for fall among hospitalized children in a specialized children’s hospital in Saudi Arabia
por: AlSowailmi, Banan Abdullah, et al.
Publicado: (2018)

Canaliculitis: Are we missing the diagnosis?
por: Al-Mujaini, Abdullah, et al.
Publicado: (2009)

Noninflammatory disorders mimic juvenile idiopathic arthritis
por: Al-Mayouf, Sulaiman M.
Publicado: (2018)

Symptomatic congenital heart disease in the Saudi Children and Adolescents Project
por: Alqurashi, Mansour, et al.
Publicado: (2007)

Chronic recurrent multifocal osteomyelitis: a first report from Saudi Arabia
por: Al Hajry, Maryam, et al.
Publicado: (2012)

Acute fulminant cholestatic jaundice in sickle cell disease
por: Al-Suleiman, Ahmad M., et al.
Publicado: (2006)

Intestinal lymphangiectasia in a patient with infantile systemic hyalinosis syndrome: a rare cause of protein-losing enteropathy
por: Alreheili, Khalid, et al.
Publicado: (2012)

Delayed diagnosis of sarcoidosis is common in Brazil
por: Rodrigues, Mauri Monteiro, et al.
Publicado: (2013)

Fructose-1,6-bisphosphatase deficiency with confirmed molecular diagnosis: An important cause of hypoglycemia in children
por: Salih, Rihab M., et al.
Publicado: (2020)

A screening tool for attention deficit hyperactivity disorder in children in Saudi Arabia
por: Hassan, Ahmad M., et al.
Publicado: (2009)

Sarcoidosis Presenting as a Penile Lesion: A Case Report
por: Al-Riyami, Hana Ali, et al.
Publicado: (2020)

Central nervous system and spinal tuberculosis in children at a tertiary care center in Saudi Arabia
por: Al Ayed, Mohammed, et al.
Publicado: (2013)

Delayed Hemolytic Transfusion Reaction in Sickle Cell Disease: A Case Series
por: Alwaheed, Abrar J., et al.
Publicado: (2022)

Coexistence of pulmonary tuberculosis with pulmonary sarcoidosis and skin sarcoidosis: a case report
por: Yusuf, Khalifa Abdulrahman, et al.
Publicado: (2023)

Delayed diagnosis in the maxillofacial region: Two case reports
por: Zain-Alabdeen, Ebtihal H., et al.
Publicado: (2017)

Acute psychosis in children: do not miss immune-mediated causes
por: AlHakeem, Afnan S., et al.
Publicado: (2016)

Combination of tacrolimus and mycophenolate mofetil in persistent proteinuria due to refractory childhood lupus nephritis
por: Almutairi, Abdulaziz, et al.
Publicado: (2018)

Treatment of Multiorgan Sarcoidosis With Tofacitinib
por: Damsky, William, et al.
Publicado: (2020)

Diagnosis of a missed central line guidewire using critical care ultrasound
por: Al Bshabshe, Ali
Publicado: (2016)

Unusual Case of Scalp Sarcoidosis with Alopecia: An Only Manifestation of Cutaneous Sarcoidosis without Systemic Involvement
por: Kim, Jin Cheol, et al.
Publicado: (2022)

Rhizomelic chondrodysplasia punctata: A missed opportunity for early diagnosis
por: Chhavi, Nanda, et al.
Publicado: (2012)

The SLC29A3 variant, neutrophilic dermatosis, and hyperferritinemia imitate systemic juvenile idiopathic arthritis in a Saudi child: a case report
por: Alansari, Shahad, et al.
Publicado: (2023)

Diffuse alveolar hemorrhage secondary to sarcoidosis
por: Diaz-Menindez, Maximiliano, et al.
Publicado: (2023)

Sarcoidosis in the Middle East
por: Jayakrishnan, B., et al.
Publicado: (2019)

Beyond a routine blood gas, an easily picked but missed diagnosis of chronic Encephalopathy
por: AlFaris, Haya S., et al.
Publicado: (2021)

The Efficacy of Yttrium-90 Radiosynovectomy in Patients with Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome
por: Al-Mayouf, Sulaiman Mohammed, et al.
Publicado: (2017)

Eosinophilic Enteritis: A Delayed Diagnosis
por: Munjal, Ankita, et al.
Publicado: (2017)

Cannot write session to /tmp/vufind_sessions/sess_2mntpgbr72ngrvj702ndoi2fpr