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  2. Progeria - Wikipedia

    en.wikipedia.org/wiki/Progeria

    Most children with progeria appear normal at birth and during early infancy. [11] Children with progeria usually develop the first symptoms during their first few months of life. The earliest symptoms may include a failure to thrive and a localized scleroderma-like skin condition. As a child ages past infancy, additional conditions become ...

  3. Fibrodysplasia ossificans progressiva - Wikipedia

    en.wikipedia.org/wiki/Fibrodysplasia_ossificans...

    Fibrodysplasia ossificans progressiva (/ ˌ f aɪ b r oʊ d ɪ ˈ s p l eɪ ʒ (i) ə ɒ ˈ s ɪ f ɪ k æ n z p r ə ˈ ɡ r ɛ s ɪ v ə /; [1] abbr. FOP), also called Münchmeyer disease or formerly myositis ossificans progressiva, is an extremely rare connective tissue disease in which fibrous connective tissue such as muscle, tendons, and ligaments turn into bone tissue (ossification).

  4. Burkholderia gladioli - Wikipedia

    en.wikipedia.org/wiki/Burkholderia_gladioli

    Burkholderia gladioli is a species of aerobic gram-negative rod-shaped bacteria [1] that causes disease in both humans and plants. It can also live in symbiosis with plants and fungi [2] and is found in soil, water, the rhizosphere, and in the microbiome of many animals.

  5. Stem cell theory of aging - Wikipedia

    en.wikipedia.org/wiki/Stem_cell_theory_of_aging

    The number of stem cells in young people is very much higher than older people and thus creates a better and more efficient replacement mechanism in the young contrary to the old. In other words, aging is not a matter of the increase in damage, but a matter of failure to replace it due to a decreased number of stem cells.

  6. Macrocephaly - Wikipedia

    en.wikipedia.org/wiki/Macrocephaly

    Macrocephaly is a condition in which circumference of the human head is abnormally large. [1] It may be pathological or harmless, and can be a familial genetic characteristic. . People diagnosed with macrocephaly will receive further medical tests to determine whether the syndrome is accompanied by particular disorde

  7. Trinucleotide repeat expansion - Wikipedia

    en.wikipedia.org/wiki/Trinucleotide_repeat_expansion

    SMBA is the first "CAG / polygutamine" disease, which is a subcategory of repeat disorders. [9] In 1992, for myotonic dystrophy type 1 (DM1), CTG expansion was found in the myotonic dystrophy protein kinase (DMPK) 3' UTR. In 1993, for Huntington's disease (HD), a longer-than-usual CAG repeat with was found in the exon 1 coding sequence. [10]

  8. Epidemiological transition - Wikipedia

    en.wikipedia.org/wiki/Epidemiological_transition

    A revised transition model might focus more on disease aetiology and the determinants of cause-specific mortality change, while encompassing the possibility that infectious causation may be established for other morbid conditions through the vast amount of ongoing research into associations with infectious diseases.

  9. Infection - Wikipedia

    en.wikipedia.org/wiki/Infection

    Primary pathogens cause disease as a result of their presence or activity within the normal, healthy host, and their intrinsic virulence (the severity of the disease they cause) is, in part, a necessary consequence of their need to reproduce and spread. Many of the most common primary pathogens of humans only infect humans, however, many ...