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  2. The Merck Manuals - Wikipedia

    en.wikipedia.org/wiki/The_Merck_Manuals

    The Merck Manuals (outside the U.S. and Canada: The MSD Manuals; Chinese: 默沙东诊疗手册; pinyin: Mòshādōng Zhěnliáo Shǒucè) are medical references published by the American pharmaceutical company Merck & Co. (known as MSD outside the United States and Canada), that cover a wide range of medical topics, including disorders, tests, diagnoses, and drugs.

  3. Metachromatic leukodystrophy - Wikipedia

    en.wikipedia.org/wiki/Metachromatic_leukodystrophy

    Presymptomatic patients can be cured with one treatment of atidarsagene autotemcel, which is a type of advanced medicine called a ‘gene therapy’. This type of medicine works by delivering genes into the body. The active substance in atidarsagene autotemcel is CD34+ stem cells. They are retrieved from the patient's own bone marrow or blood.

  4. Duchenne muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Duchenne_muscular_dystrophy

    Duchenne muscular dystrophy (DMD) is a severe type of muscular dystrophy predominantly affecting boys. [ 3 ] [ 7 ] [ 8 ] The onset of muscle weakness typically begins around age four, with rapid progression. [ 2 ]

  5. Deflazacort - Wikipedia

    en.wikipedia.org/wiki/Deflazacort

    The U.S. Food and Drug Administration approved deflazacort to treat people age five years and older with Duchenne muscular dystrophy (DMD), a rare genetic disorder that causes progressive muscle deterioration and weakness. Emflaza is a corticosteroid that works by decreasing inflammation and reducing the activity of the immune system. [5]

  6. Muscular dystrophy - Wikipedia

    en.wikipedia.org/wiki/Muscular_Dystrophy

    In the 1860s, descriptions of boys who grew progressively weaker, lost the ability to walk, and died at an early age became more prominent in medical journals. In the following decade, [ 33 ] French neurologist Guillaume Duchenne gave a comprehensive account of the most common and severe form of the disease, which now carries his name ...

  7. Multiple sulfatase deficiency - Wikipedia

    en.wikipedia.org/wiki/Multiple_sulfatase_deficiency

    25% (1 in 4) children will be free of MSD - unaffected child that is not a carrier; If one parent is affected and one is free of MSD: 0% (0) children will have the disorder - only one parent is affected, other parent always gives normal gene; 100% (4 in 4) children will be carriers (but unaffected)

  8. Musculoskeletal disorder - Wikipedia

    en.wikipedia.org/wiki/Musculoskeletal_disorder

    Doctors rely on medical history, recreational and occupational hazards, intensity of pain, a physical exam to locate the source of the pain, and sometimes lab tests, X-rays, or an MRI [21] Doctors look for specific criteria to diagnose each different musculoskeletal disorder, based on location, type, and intensity of pain, as well as what kind ...

  9. Merck Manual of Diagnosis and Therapy - Wikipedia

    en.wikipedia.org/wiki/Merck_Manual_of_Diagnosis...

    The first edition of The Merck Manual was published in 1899 by Merck & Co., Inc. for physicians and pharmacists and was titled Merck's Manual of the Materia Medica. [6] [7] The 192 page book which sold for US $1.00, was divided into three sections, Part I ("Materia Medica") was an alphabetical listing of all known compounds thought to be of therapeutic value with uses and doses; Part II ...