Mindblown: a blog about philosophy.

  • Masa syndrome

    MASA syndrome is a rare hereditary, X-linked recessive disorder that has specific, progressively appearing neurological and clinical signs. MASA is the acronym for the four main characteristics that delineate the syndrome (mental retardation, aphasia, shuffling gait, and adducted thumbs). MASA syndrome is often used interchangeably with CRASH syndrome (also named for its characteristics), which are…

  • Marshall-smith syndrome

    Marshall-Smith syndrome (MSS) is a nonhereditary disorder of increased skeletal growth, accelerated maturation and an extensive assortment of associated defeats. MSS has its onset during fetal development. Abnormal findings are quite obvious in the newborn.  

  • Marinesco-sjogren syndrome

    Marinesco-Sjogren syndrome (MSS) is an hereditary neuromuscular disorder. Associated defects are common in the eye and skeleton.  

  • Marijuana abuse

    Marijuana is the term used to describe the mixture of dried, shredded leaves and flowers of Cannabis sativa, or hemp plant. There are many slang terms for marijuana, including pot, grass, weed, reefer, boom, and gangster. Marijuana is generally smoked in the form of loosely rolled cigarettes (joints) or hollowed-out cigars filled with marijuana (blunts).…

  • Marden-walker syndrome

    Marden-Walker syndrome (MWS) is an extremely rare autosomal recessive connective tissue disorder. Medical and cognitive implications associated with this syndrome have onset at birth. Although this statistic is tentative, the prevalence of MWS has been estimated at less than 1 birth per 1,000,000. With regard to gender, MWS is approximately twice as frequent in males…

  • Mannosidosis

    Alpha-mannosidosis is a rare metabolic disorder characterized by a deficiency of the lysosomal enzyme alpha- mannosidase. Due to this deficiency, oligosaccharides accumulate within cells of body tissues. Symptoms of the disorder vary widely, as does severity. There are two forms of alpha-mannosidosis. Type I typically develops in early childhood, with age of onset ranging from…

  • Maffucci syndrome

    Maffucci syndrome (MS) is a nonhereditary disorder of skeletal and vascular tissues. Its salient features include benign tumors of cartilage and bone (enchondromas) and blood vessel malformations (hemangiomas). A condition marked by the presence of enchondromas (noncancerous cartilage tumors) along with hemangiomas (noncancerous blood vessel tumors) on the skin or within internal organs. This syndrome…

  • Lymphangioleiomyomatosis

    Lymphangioleiomyomatosis is a very rare (although predominantly found in women of childbearing age, childhood cases have been reported), progressive lung disease characterized by misdifferentiated unusual muscle cells that invade lung tissue and blood and lymph vessels. Leiomyomatosis, resultant from LAM, form to create bundles growing into the lung walls, blood and lymph vessels, obstructing these…

  • Lujan-fryns syndrome

    Lujan-Fryns Syndrome (LFS) is a very low-incidence, X- linked disorder that is characterized primarily by the presence of a tall yet stooped posture, hyperextensible fingers and toes, large forehead, long yet narrow face that includes an extended nose with a high bridge, thin upper lip, arched palate, and maxillary hypoplasia. A review and report of…

  • Lowe syndrome

    First described in 1952, Lowe syndrome is an X-linked recessive (chromosome location Xq26.1) disorder, of unknown etiology resulting in an ocular, cerebral, and renal syndrome. The incidence of Lowe syndrome is rare (about 50 cases worldwide), and males are at more risk than females. Lowe’s syndrome is an infrequent genetic disorder that follows an X-linked…

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