Case report and review of delayed-interval delivery for dichorionic, diamniotic twins with normal development

2012 ◽  
Vol 38 (4) ◽  
pp. 741-744 ◽  
Author(s):  
Masatoki Kaneko ◽  
Yasuyuki Kawagoe ◽  
Junji Oonishi ◽  
Naoshi Yamada ◽  
Hiroshi Sameshima ◽  
...  
2016 ◽  
Vol 33 (S1) ◽  
pp. S154-S154
Author(s):  
E. Garcia ◽  
I. Vicente ◽  
R. Martínez

We comment the case of a 12 years old girl who started with visual and auditive hallucinations. Hallucinations are not a common symptom between children. They may also be linked to many conditions, some of them with poor outcome as schizophrenia. Symptoms appeared in a short time, after a previous normal development. She talked about a man who followed her and that was always behind, she also had heard some insults of undeterminated voices. These symptoms were just of one-month duration and made her feel anxious and very afraid. After a normal organical study and a first proposal of medication they asked for our consultation. We found that the patient was alone at home every afternoon. Family, from other country, hadn’t any social support, and the father had had to travel away some days before the child began to suffer hallucinations. Suspecting an affective disorder as the basis of anxious symptoms, and hallucinations as a cultural presentation of them, we started with a social intervention mixed with support therapy. After some sessions the patient could talk about her loneliness and fears, disappearing the other symptoms. We will resume this case and literature about other cultural presentations that may difficult diagnosis or treatment.Disclosure of interestThe authors have not supplied their declaration of competing interest.


2020 ◽  
pp. 014556132094463
Author(s):  
Huiying Sun ◽  
Yufei Qiao ◽  
Na Chen ◽  
Hua Yang ◽  
Zhiqiang Gao ◽  
...  

We report a 6-year-old girl with progressive bilateral conductive hearing loss for 2 years. She passed the newborn hearing screening conducted with otoacoustic emissions testing and had a normal development of speech and language, which indicated that her deafness was delayed-onset. She also had congenital proximal interphalangeal joints. Proximal symphalangism was confirmed by genetic testing ( NOG gene: c.406C > T, p.R136C). Bilateral stapes ankyloses were proved by surgery and her hearing was improved after stapedotomy by over 30 dB. Besides, this case should remind clinicians to carefully distinguish NOG gene-related deafness from congenital ossicular malformation and pediatric otosclerosis.


1993 ◽  
Vol 8 (4) ◽  
pp. 649-651 ◽  
Author(s):  
A. Fignon ◽  
S. Hamamah ◽  
G. Body ◽  
D. Royere ◽  
F. Gold ◽  
...  

2013 ◽  
Vol 98 (Suppl 1) ◽  
pp. A106.3-A106
Author(s):  
J O’Neill ◽  
A Ahmed ◽  
D Hayes-Ryan ◽  
E O’Donnell

2019 ◽  
Vol 58 (4) ◽  
pp. 579-580 ◽  
Author(s):  
Erdogan Nohuz ◽  
Maël Albaut ◽  
Marie Szymanowski ◽  
Angélique Brunel ◽  
Didier Lemery ◽  
...  

2019 ◽  
Vol 20 ◽  
pp. 739-742 ◽  
Author(s):  
Suzanne Cao ◽  
Logan Walter ◽  
Guillermo J. Valenzuela ◽  
Kristina Roloff

1961 ◽  
Vol 107 (450) ◽  
pp. 931-935 ◽  
Author(s):  
John Johnson

The first clinical histories of this condition were reported in Norway by Stengel (1826). Batten (1903) described changes in the macula in two members of a family who had undergone progressive mental deterioration with loss of visual and motor functions. Vogt (1906) published similar cases and attempted to delimit them as a juvenile form of Tay Sachs disease. It differed from the infantile form in that it occurred in childhood after a period of normal development; the rate of progression was slower; it was not limited to Jewish children and the ophthalmological appearances were those of optic atrophy. The following year Spielmeyer described the pathological changes in juvenile Tay Sachs disease as essentially similar to the infantile form. Further detailed pathological studies were made by Greenfield and Holmes (1925).


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