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  2. Proteus syndrome - Wikipedia

    en.wikipedia.org/wiki/Proteus_syndrome

    Proteus syndrome is a rare genetic disorder [1] that can cause tissue overgrowth involving all three embryonic lineages. Patients with Proteus syndrome tend to have an increased risk of embryonic tumor development. [2] The clinical symptoms and radiographic findings of Proteus syndrome are highly variable, as are its orthopedic manifestations ...

  3. Bannayan–Riley–Ruvalcaba syndrome - Wikipedia

    en.wikipedia.org/wiki/Bannayan–Riley...

    Bannayan–Riley–Ruvalcaba syndrome; Other names: BRRS: Autosomal dominant is the manner in which this condition is inherited: Specialty: Oncology, medical genetics Symptoms: Enlarged head [1] Causes: Mutations in the PTEN gene [2] Diagnostic method: Based on signs and symptoms [3] Treatment: Based on symptoms [3]

  4. Overgrowth syndrome - Wikipedia

    en.wikipedia.org/wiki/Overgrowth_syndrome

    Children with some overgrowth syndromes such as Klippel–Trénaunay syndrome can be readily detectable at birth. [3] In contrast, other overgrowth syndromes such as Proteus syndrome usually present in the postnatal period, characteristically between the second and third year of life. [2]

  5. PIK3CA-related overgrowth spectrum - Wikipedia

    en.wikipedia.org/wiki/PIK3CA-related_overgrowth...

    Treatment of PROS diseases is variable and depends on the specific disease. Curative treatment does not exist and most treatments are given to control symptoms. Overgrowth and malformations of solid tissues can be treated with surgery. Sclerotherapy can be used to treat vascular malformations. [5]

  6. Proteus-like syndrome - Wikipedia

    en.wikipedia.org/wiki/Proteus-like_syndrome

    Proteus-like syndrome (PLS) is a condition similar to Proteus syndrome, but with an uncertain cause. [1] It's characterized by skeletal and hamartous overgrowth of multiple tissues, nevi in cerebriform connective tissue, blood vessel malformations and linear epidermal nevi.

  7. Phakomatosis - Wikipedia

    en.wikipedia.org/wiki/Phakomatosis

    The treatment of each neurocutaneous syndrome is unique. For some neurocutaneous syndromes such as neurofibromatosis 1 and tuberous sclerosis complex there are guidelines with recommendations for surveillance and management. [78] [79] For less common syndromes such guidelines are not yet available. Surveillance is a necessity for many ...

  8. Infantile hemangioma - Wikipedia

    en.wikipedia.org/wiki/Infantile_hemangioma

    Multidisciplinary clinical practice guidelines for the management of infantile hemangiomas were recently published. [42] Indications for treatment include functional impairment (i.e. visual or feeding compromise), bleeding, potentially life-threatening complications (airway, cardiac, or hepatic disease), and risk of long-term or permanent ...

  9. Klippel–Trénaunay syndrome - Wikipedia

    en.wikipedia.org/wiki/Klippel–Trénaunay_syndrome

    This can cause pain, swelling, inflammations, and in some cases, even ulceration and infection. Among older children and adults, compression garments can be used to alleviate almost all of these, and when combined with elevation of the affected area and proper management, can result in a comfortable lifestyle for the patient without any surgery ...