scholarly journals The assessment of cognitive function in a Williams syndrome patient: A case report

2004 ◽  
Vol 58 (1) ◽  
pp. 99-99 ◽  
Author(s):  
TOMOO NAMIHIRA ◽  
YOSHIO HIRAYASU ◽  
YOSHIHIKO KOGA
2018 ◽  
Vol 4 (1) ◽  
Author(s):  
Mubashir Alavi Jusabani ◽  
Sakina Mehboob Rashid ◽  
Honest Herman Massawe ◽  
William Patrick Howlett ◽  
Marieke Cornelia Johanna Dekker

2020 ◽  
Vol 32 (1) ◽  
pp. 5-8
Author(s):  
David Hersey

A 39-year-old male, who attempted suicide by hanging, developed chronic myoclonus with intact cognitive function. Chronic post-hypoxic myoclonus is a rare syndrome that may develop after a respiratory arrest and it presents as late onset and persistent purposeful myoclonus with preserved or slightly impaired cognitive function. Increasing critical care nurses’ awareness of chronic post-hypoxic myoclonus will lead to earlier diagnosis of this rare syndrome.


2006 ◽  
Vol 51 (3) ◽  
pp. 371
Author(s):  
Kyu Don Chung ◽  
Youn Suk Son ◽  
Sang Hyun Hong ◽  
Hyun Sook Cho

2020 ◽  
Vol 30 (4) ◽  
pp. 568-570 ◽  
Author(s):  
Thomas S. Davis ◽  
Monica S. Epelman ◽  
Peace C. Madueme ◽  
Karen S. Bender ◽  
Gul H. Dadlani

AbstractWilliams syndrome is a multisystem, congenital disorder which is commonly associated with arterial stenoses: supravalvar aortic stenosis and peripheral pulmonary artery stenosis. Venous abnormalities have not been previously reported in children with Williams syndrome. We present a case of a 3-year-old girl with Williams syndrome and diffuse venous ectasia as detected by MRI.


2016 ◽  
Vol 16 (10) ◽  
pp. 1171-1172
Author(s):  
Satoru Morimoto ◽  
Jun Tanaka ◽  
Yoko Saito ◽  
Naoko Tsuyama ◽  
Takashi Nishimura ◽  
...  

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