Lymphedema–distichiasis syndrome is a medical condition associated with the FOXC2 gene.: 849 People with this hereditary condition have a double row of...
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syndrome, lymphedema–distichiasis syndrome, yellow nail syndrome, and Klippel–Trénaunay syndrome. One defined genetic cause for hereditary lymphedema...
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syndrome Lujan–Fryns syndrome Lutembacher's syndrome Lymphangitis carcinomatosa Lymphedema–distichiasis syndrome Lynch syndrome Lyngstadaas syndrome Löffler's...
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form of primary lymphedema, accounting for about 80% of the patients.: 848 Lymphedema Lymphedema-distichiasis syndrome Aagenaes syndrome List of cutaneous...
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of a study published in 1968, were alive at the time. Lymphedema-distichiasis syndrome Lymphedema praecox Blueberry muffin baby Rapini, Ronald P.; Bolognia...
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the lower extremities Lymphedema–distichiasis syndrome, a genetic disorder of eyelashes and lymphatic system Loeys–Dietz syndrome, a genetic disorder affecting...
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neoplasm Lymphedema distichiasis Lymphedema hereditary type 1 Lymphedema hereditary type 2 Lymphedema ptosis Lymphedema, congenital Lymphedema Lymphedema–distichiasis...
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Campomelic dysplasia (redirect from Camptomelic syndrome)
FOXC1 Axenfeld syndrome 3 Iridogoniodysgenesis, dominant type FOXC2 Lymphedema–distichiasis syndrome FOXE1 Bamforth–Lazarus syndrome FOXE3 Anterior segment...
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Pitt–Hopkins syndrome (PTHS) is a rare genetic disorder characterized by developmental delay, epilepsy, distinctive facial features, and possible intermittent...
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syndrome, segmental hyalinizing vasculitis) Lymphedema praecox Lymphedema–distichiasis syndrome Maffucci syndrome Majocchi's disease (purpura annularis telangiectodes...
198 KB (17,977 words) - 12:52, 16 May 2024
lymphedema-distichiasis syndrome". Lymphology. 43 (1): 14–8. PMID 20552815. Witte MH, Erickson RP, Khalil M, et al. (2009). "Lymphedema-distichiasis syndrome...
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laxa FOXC2 Lymphedema–distichiasis syndrome Meige lymphedema GALNT3 Familial tumoral calcinosis GJB2 Connexin 26 KID syndrome Vohwinkel syndrome Bart–Pumphrey...
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Latex allergy (I+IV) Autoimmune Sjögren's syndrome Autoimmune hepatitis Autoimmune polyendocrine syndrome (APS1 / APS2) Autoimmune adrenalitis Systemic...
38 KB (2,656 words) - 12:11, 30 October 2023
somatic; 606690; TSC2 Lymphedema, hereditary I; 153100; FLT4 Lymphedema, hereditary, IC; 613480; GJC2 Lymphedema–distichiasis syndrome with renal disease...
234 KB (18,877 words) - 15:43, 9 May 2024