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  3. Research By Disease

Disease: Hornova Dlurosova syndrome

  • A case of congenital nephrotic syndrome detected during screening for congenital hypothyroidism
  • Combination surgery (ECCE+IOL+TE) and intraocular pressure levels
  • Correlation of clinical, surgical and histopathological findings in temporomandibular arthropathies
  • Evaluation of the Effectiveness of Teduglutide Treatment in Patients with Short Bowel Syndrome in Slovakia-Multicenter Real-World Study
  • Examination of the structure and surface of articular disc in surgically treated arthropathies
  • Intrathecal baclofen in mucopolysaccharidosis type II (Hunter syndrome): case report
  • Lymphosarcoma of the parotid gland in Sjogren syndrom
  • Neonatal hypoglycemia, early-onset diabetes and hypopituitarism due to the mutation in EIF2S3 gene causing MEHMO syndrome
  • Polyhormonal immunopathogenetic syndromes and mechanisms of their origins
  • Proteohormones as markers of malignant tumors. Paraneoplastic endocrine syndromes
  • Radiotherapy and radiosensitivity syndromes in DNA repair gene mutations
  • Study on the polyglandular immunogenic insufficiency of endocrine glands (Schmidt's syndrome)
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About CheckOrphan

CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity.
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