When sleep-related hypermotor epilepsy (SHE) met Charles Darwin and Francis Galton

Neurology ◽  
2017 ◽  
Vol 89 (5) ◽  
pp. 502-505 ◽  
Author(s):  
Liborio Parrino ◽  
Giovanni Pavesi

Sleep-related hypermotor epilepsy (SHE) is characterized by short-lasting seizures patterned by repetitive and stereotyped motor events in the same person. In autosomal dominant SHE, genetic factors play a well-known key role. In The Expression of Emotions in Man and Animals, Charles Darwin quotes a plausible example of SHE illustrated by his cousin Sir Francis Galton: “the gentleman…lay fast asleep on his back in bed, raising his right arm slowly in front of his face, up to his forehead, and then dropping it with a jerk, so that the wrist fell heavily on the bridge of his nose. The trick did not occur every night, but occasionally, and was independent of any ascertained cause. Sometimes it was repeated incessantly for an hour or more.” Similar manifestations during sleep occurred also in the patient's son and granddaughter, suggesting an autosomal inheritance without sex relationship. Differential diagnosis with REM behavior disorder and other parasomnias is discussed. To our knowledge, this could be the first description of a stereotyped SHE pattern with genetic transmission.

2020 ◽  
Vol 78 (10) ◽  
pp. 601-602
Author(s):  
Dalva POYARES ◽  
Ronaldo Delmonte PIOVEZAN

Author(s):  
Monica F Cohen

Abstract This story traces the many adventures of a title, from Edward Jenkins’s 1870 novel, Ginx’s Baby, through colonial resistance to imperial copyright law in Canada, to the photograph of a distressed baby that Charles Darwin featured in The Expression of Emotions in Man and Animals and that the art photographer Oscar Rejlander reproduced as popular cartes de visites. The reiterative use of the title across genres and oceans conjures an image of Victorian popular culture as an unregulated bazaar affording the surprising emergence of unintended creators. Copyright history, frame analysis, and name theory help explain how the title of a popular novel could lend itself to so many unrelated creative objects.


Author(s):  
Tivya Kulasegaran ◽  
Pranav Kumar

Familial hypocalciuric hypercalcaemia (FHH) is a rare genetic autosomal dominant disorder, with 3 variants described. An inactivating mutation in the calcium sensor receptor (CASR) gene causes the subtype 1, which represents 65% of the cases. Inactivation of Ca-sensing receptors (CaSR) can also lead to hypercalcemia associated with increased parathyroid hormone (PTH) secretion.[1] It is characterised by causes mild asymptomatic hypercalcemia[2] and hypocalciuria with normal or elevated PTH. FHH is generally asymptomatic and treatment is not needed. Differential diagnosis with primary hyperparathyroidism (PHPT) is crucial and based on calcium-creatinine clearance ratio (CCCR), which, when under 0.02 points to the diagnosis of FHH.[3] Genetic test is necessary for confirmation.[4]


Genes ◽  
2021 ◽  
Vol 12 (12) ◽  
pp. 1855
Author(s):  
Justyna Chojdak-Łukasiewicz ◽  
Edyta Dziadkowiak ◽  
Sławomir Budrewicz

Strokes are the main cause of death and long-term disability worldwide. A stroke is a heterogeneous multi-factorial condition, caused by a combination of environmental and genetic factors. Monogenic disorders account for about 1% to 5% of all stroke cases. The most common single-gene diseases connected with strokes are cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) Fabry disease, mitochondrial myopathy, encephalopathy, lactacidosis, and stroke (MELAS) and a lot of single-gene diseases associated particularly with cerebral small-vessel disease, such as COL4A1 syndrome, cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL), and Hereditary endotheliopathy with retinopathy, nephropathy, and stroke (HERNS). In this article the clinical phenotype for the most important single-gene disorders associated with strokes are presented. The monogenic causes of a stroke are rare, but early diagnosis is important in order to provide appropriate therapy when available.


Parasomnias ◽  
2013 ◽  
pp. 221-235
Author(s):  
Sujay Kansagra ◽  
Bradley V. Vaughn

2021 ◽  
Vol 51 (12) ◽  
pp. 582-588
Author(s):  
Usman Riaz ◽  
Jacob Gohari ◽  
Syed Ali Riaz

2021 ◽  
Vol 429 ◽  
pp. 118662
Author(s):  
Samantha Mombelli ◽  
Caterina Leitner ◽  
Marco Sforza ◽  
Andrea Galbiati ◽  
Giada D'Este ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document