Results 1 to 10 of about 7,368 (202)

Beyond Cystic Fibrosis: Recognising Shwachman‐Diamond Syndrome in the Respiratory Clinic [PDF]

open access: yesRespirology Case Reports
Cystic fibrosis (CF) and Shwachman‐Diamond Syndrome (SDS) share overlapping features, including recurrent respiratory infections and pancreatic insufficiency, which can complicate diagnosis.
Freda Yang   +3 more
doaj   +4 more sources

Clinical features, epidemiology, and treatment of Shwachman-Diamond syndrome: a systematic review [PDF]

open access: yesBMC Pediatrics, 2023
Background Shwachman-Diamond syndrome (SDS) is an autosomal recessive disease which results in inherited bone marrow failure (IBMF) and is characterized by exocrine pancreatic dysfunction and diverse clinical phenotypes. In the present study, we reviewed
Xue Han   +5 more
doaj   +3 more sources

Constitutive systemic inflammation in Shwachman-Diamond Syndrome [PDF]

open access: yesMolecular Medicine
Background and purpose Shwachman-Diamond Syndrome (SDS) is an autosomal recessive disease belonging to the inherited bone marrow failure syndromes and characterized by hypocellular bone marrow, exocrine pancreatic insufficiency, and skeletal ...
Giuseppe Sabbioni   +13 more
doaj   +3 more sources

Spectrum of diabetes mellitus in patients with Shwachman-Diamond syndrome: case report and review of the literature [PDF]

open access: yesItalian Journal of Pediatrics, 2023
Background Shwachman-Diamond syndrome (SDS) is a rare congenital disorder caused by mutations in the SBDS gene and characterized by exocrine pancreatic deficiency, hematologic dysfunction, and skeletal growth failure.
Lusine V. Navasardyan   +5 more
doaj   +3 more sources

Reduced EIF6 dosage attenuates TP53 activation in models of Shwachman-Diamond syndrome [PDF]

open access: yesThe Journal of Clinical Investigation
Shwachman-Diamond syndrome (SDS) is characterized by neutropenia, exocrine pancreatic insufficiency, and bony abnormalities with an increased risk of myeloid neoplasia.
Usua Oyarbide   +7 more
doaj   +3 more sources

Shwachman Diamond Syndrome with Arrhythmia as the First Manifestation a Case Report and Literature Review [PDF]

open access: yesPharmacogenomics and Personalized Medicine, 2022
Hang Yu,1,* Wenwei Zhao,2,* Yongqing Ni,1,* Linlin Li1,* 1Department of Pediatric, The Affiliated Hospital of Inner Mongolia Medical University, Hohhot, Inner Mongolia Autonomous Region, 010030, People’s Republic of China; 2Office of the ...
Yu H, Zhao W, Ni Y, Li L
doaj   +3 more sources

Case Report: A case report and literature review of shwachman-diamond syndrome concurrent with klinefelter syndrome [PDF]

open access: yesFrontiers in Pediatrics
Shwachman-Diamond syndrome (SDS) is a rare genetic disorder characterized by pancreatic insufficiency, metaphyseal chondrodysplasia, and bone marrow failure.
Chenyang Chang   +17 more
doaj   +3 more sources

Ataluren improves hematopoietic and pancreatic disorders in Shwachman-Diamond syndrome patients: a compassionate program case-series [PDF]

open access: yesNature Communications
Shwachman-Diamond syndrome (SDS) is characterized by exocrine pancreatic insufficiency, neutropenia, and a high risk of myeloid malignancy. Most patients with SDS harbor nonsense mutations in Shwachman-Bodian-Diamond syndrome gene (SBDS), which encodes a
Valentino Bezzerri   +19 more
doaj   +3 more sources

Distinct genetic pathways define pre-malignant versus compensatory clonal hematopoiesis in Shwachman-Diamond syndrome

open access: yesNature Communications, 2021
Understanding the molecular basis of leukaemia predisposition is essential for intervention. The authors here investigate germline genetic leukaemia predisposition by studying Shwachman-Diamond syndrome and report compensatory inactivating mutations in ...
Alyssa L. Kennedy   +42 more
doaj   +2 more sources

Classification of and risk factors for hematologic complications in a French national cohort of 102 patients with Shwachman-Diamond syndrome [PDF]

open access: yesHaematologica, 2012
Background Patients with the Shwachman-Diamond syndrome often develop hematologic complications. No risk factors for these complications have so far been identified.
Jean Donadieu   +20 more
doaj   +6 more sources

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