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USMLE AID on X: "William's syndrome Chromosome 7 mutation(long arm) Presenting with Elfin facies https://t.co/OadeLJqwSe" / X
Medical Addicts - Info: William's syndrome Although it's a rare neurodevelopmental disorder (about 1 in 7,500 to 1 in 20,000 births) but believe me , when you meet a patient with such
Characteristic "elfin facies" in 1 of our patients, showing... | Download Scientific Diagram
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Williams Syndrome, Williams Beuren Syndrome: Causes, Symptoms & Treatment
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Typical "elfin face". Williams' syndrome children show few peculiar... | Download Scientific Diagram
Sthanu on X: "Elfin facies characteristic facial appearance seen in certain rare congenital syndromes. Elfin facies is sometimes used synonymously with Williams syndrome and the latter is occasionally called elfin facies syndrome
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Alt Shift X on X: "In the Dune books, Chani is described as a “girl-child” with an “elfin face”, “darkly elfin” features, and “red hair”. https://t.co/gVaLSHy3hb" / X
Elfin facies / William Syndrome facial characteristics #medical #medicine # face #shorts #reels - YouTube
Pedia4PG by Dr Sidharth Sethi - NEET PG 2020 William's Syndrome- deletion 7q11.23 [Told in all DAMS Pediatrics classes since 15 yrs!] The Williams syndrome is a sporadic disorder generally characterized by
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Toddler With Elfin Face, Cardiovascular Abnormalities, Hypercalcemia, and Developmental Delays | Consultant360
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