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American Journal of Rare Disorders: Diagnosis & Therapy (AJRDDT) is an Open Access peer reviewed, online publishing journal which aims to publish scholarly and quality papers in the significant areas of current Rare Disorders.

A Rare Disorders is any disease that influences a fraction of the population. The majority of Rare Disorders is genetic, and thus is present throughout the person's entire life, even if symptoms do not immediately appear.

Aims and Scope

American Journal of Rare Disorders: Diagnosis & Therapy aim is to publish articles on related aspects of public health, health policy and clinical investigation, which can progress health care and outcomes for people suffering from Orphan diseases, furthermore to increase rare diseases expertise worldwide on rare diseases actions, analysis, treatment and prevention. The highlights on novel clinical features, clinical report, rare case information, Molecular genetics etiology, pathogenesis, molecular environmental science, health economics and health management of rare diseases.

Article Types

American Journal of Rare Disorders: Diagnosis & Therapy (AJRDDT) publishes Original research articles, clinical trials, Reviews, Case report, Editorials, Letter to the editor, Short communication, Opinion, Book review and other special featured articles related to the field of Rare Disorders.

Please share your manuscript through online platform: online submission or as an E-mail attachment to the Editorial Office at raredisorders@scireslit.com

Scope Keywords

American Journal of Rare Disorders: Diagnosis & Therapy covers all topics related to

  • Zoonotic Diseases
  • Muscular Distropy
  • Chromosomal Abnormalities
  • Sickle Cell Anemia
  • Orphan Diseases
  • Orphan Drugs
  • Rare Autoimmune Disorders
  • Rare Bone Diseases
  • Rare Cancer
  • Rare Blood Disorders
  • Rare Endocrine Disorders
  • Rare Pediatric Diseases
  • Rare Metabolic Disorders
  • Rare Vascular Disorders
  • Rare Skin Disorders and Diseases
  • Rare Congenital Disorders
  • Facial Hemi atrophy
  • Pupil Disorder
  • Rheumatoid Arthritis
  • Acheiropodia
  • Acrodysostosis
  • Arrhinia
  • Breast hypertrophy
  • Brunner syndrome
  • Carcinosarcoma
  • Cystic fibrosis
  • Dental Townsend Siegel syndrome
  • Dahlberg Borer Newcomer syndrome
  • Dandy-Walker syndrome
  • Danon disease
  • Deficiency of the interleukin-1-receptor antagonist
  • Degos disease
  • Dent's disease
  • Denys-Drash syndrome
  • Dermatopathia pigmentosa reticularis
  • Dextrocardia
  • Diabetes insipidus
  • Diffuse panbronchiolitis
  • Diphallia
  • Dipygus
  • Donohue syndrome
  • Dracunculiasis
  • Dravet syndrome
  • Dubowitz syndrome
  • Dupuytren's contracture
  • Dysfibrinogenemia
  • Dyskeratosis congenital