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  2. Sever's disease - Wikipedia

    en.wikipedia.org/wiki/Sever's_disease

    Sever's disease is not a serious condition and many children get better without needing health professional care. If use of home treatments like putting ice on the heels or changing sport don't work, children should be assessed by a health professionals to personalise the treatment and make sure it really is calcaneal apophysitis.

  3. Severe combined immunodeficiency - Wikipedia

    en.wikipedia.org/wiki/Severe_combined...

    Severe combined immunodeficiency (SCID), also known as Swiss-type agammaglobulinemia, is a rare genetic disorder characterized by the disturbed development of functional T cells and B cells caused by numerous genetic mutations that result in differing clinical presentations. [2]

  4. Sinding-Larsen and Johansson syndrome - Wikipedia

    en.wikipedia.org/wiki/Sinding-Larsen_and...

    It is analogous to Osgood–Schlatter disease which involves the upper margin of the tibia. This variant was discovered in 1908, during a winter indoor Olympic qualifier event in Scandinavia. Sever's disease is a similar condition affecting the heel.

  5. Infantile cortical hyperostosis - Wikipedia

    en.wikipedia.org/wiki/Infantile_cortical...

    Infantile cortical hyperostosis is a self-limited condition, meaning that the disease resolves on its own without treatment, usually within 6–9 months. Long-term deformities of the involved bones, including bony fusions and limb-length inequalities, are possible but rare. [citation needed]

  6. Severe congenital neutropenia - Wikipedia

    en.wikipedia.org/wiki/Severe_Congenital_Neutropenia

    Kostmann disease, Kostmann's agranulocytosis, Kostmann's syndrome, congenital agranulocytosis, congenital neutropenia, permanent neutropenia, infantile genetic agranulocytosis, severe infantile genetic neutropenia: Specialty: Hematology Usual onset: Infancy [1] Types: SCN1-SCN5, SCNX: Causes: Mutation in genes, depending on type [1] Diagnostic ...

  7. Stevens–Johnson syndrome - Wikipedia

    en.wikipedia.org/wiki/Stevens–Johnson_syndrome

    Stevens–Johnson syndrome (SJS) is a type of severe skin reaction. [1] Together with toxic epidermal necrolysis (TEN) and Stevens–Johnson/toxic epidermal necrolysis (SJS/TEN) overlap, they are considered febrile mucocutaneous drug reactions and probably part of the same spectrum of disease, with SJS being less severe.

  8. Jarisch–Herxheimer reaction - Wikipedia

    en.wikipedia.org/wiki/Jarisch–Herxheimer_reaction

    The reaction is also seen in the other diseases caused by spirochetes: Lyme disease, relapsing fever, and leptospirosis. [4] There have been case reports of the Jarisch–Herxheimer reaction accompanying treatment of other infections, including Q fever, bartonellosis, brucellosis, trichinellosis, and African trypanosomiasis. [3]

  9. Osteomyelitis - Wikipedia

    en.wikipedia.org/wiki/Osteomyelitis

    Treatment of the relatively rare fungal osteomyelitis as mycetoma infection entails the use of antifungal medications. [9] In contrast to bacterial osteomyelitis, amputation or large bony resections is more common in neglected fungal osteomyelitis (mycetoma) where infections of the foot account for the majority of cases.