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Global Journal of Rare Diseases  Open Access

    Aims and Scope

    The Global Journal of Rare Diseases welcome manuscripts on new researches, interesting discoveries related to the rare disease community. Peertechz appeals the authors to play a distinctive role in putting forward rare diseases as a much needed public health priority world-wide.

    The Global Journal of Rare Diseases urges the prominent researchers, intensive writers and workaholic doctors to publish breakthrough manuscripts with Peertechz that can lead the way to studies leading to education, research and advocacy towards patient services to improve the lives of all people living with rare diseases.

    Disciplines in Global Journal of Rare Diseases

    Authors are suggested to research, write and send manuscripts in following, but not limited to research disciplines of rare diseases and treatment:

    • Acrocephalosyndactylia
    • Acrodermatitis
    • Addison Disease
    • Adie Syndrome
    • Alagille Syndrome
    • Bardet-Biedl Syndrome
    • Barrett Esophagus
    • Beckwith-Wiedemann Syndrome
    • Behcet Syndrome
    • Bloom Syndrome
    • Bowen's Disease
    • Caroli Disease
    • Charcot-Marie-Tooth Disease
    • Chediak-Higashi Syndrome
    • Chiari-Frommel Syndrome
    • Crohn Disease
    • Cushing Syndrome
    • Cystic Fibrosis
    • De Lange Syndrome
    • Dermatitis Herpetiformis
    • DiGeorge Syndrome
    • Ebstein Anomaly
    • Eisenmenger Complex
    • Encephalitis
    • Enchondromatosis
    • Epidermal Necrolysis
    • Facial Hemiatrophy
    • Factor XII Deficiency
    • Fanconi Anemia
    • Felty's Syndrome
    • Fibrous Dysplasia
    • Gaucher Disease
    • Gerstmann Syndrome
    • Giant Lymph Node Hyperplasia
    • Glycogen Storage Disease
    • Hamartoma Syndrome
    • Hartnup Disease
    • Hepatolenticular Degeneration
    • Hodgkin Disease
    • Hyperhidrosis
    • Intestinal Polyps
    • Isaacs Syndrome
    • Kartagener Syndrome
    • Kearns-Sayre Syndrome
    • Korsakoff Syndrome
    • Lafora Disease
    • Lambert-Eaton Myasthenic Syndrome
    • Mallory-Weiss Syndrome
    • Muscular Atrophy, Spinal
    • Narcolepsy
    • Neuroaxonal Dystrophies
    • Neuromyelitis Optica
    • Neuronal Ceroid-Lipofuscinoses
    • Optic Atrophies, Hereditary
    • Osteitis Deformans
    • Osteochondritis
    • Pelizaeus-Merzbacher Disease
    • Pierre Robin Syndrome
    • Pigmentation Disorders
    • Pityriasis Lichenoides
    • Rubinstein-Taybi Syndrome
    • Sandhoff Disease
    • Spinal Muscular Atrophies of Childhood
    • Thromboangiitis Obliterans
    • Tourette Syndrome
    • Wegener Granulomatosis
    • Werner Syndrome
    • Wolff-Parkinson-White Syndrome
    • Zellweger Syndrome

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