scholarly journals Congenital Form of Isolated Benign Primary Cutaneous Plasmacytosis in a Child

2014 ◽  
Vol 26 (1) ◽  
pp. 121 ◽  
Author(s):  
Hyo Sang Song ◽  
Sue Kyung Kim ◽  
You Chan Kim
Keyword(s):  
Congenital Form

scholarly journals An Odd Keloid Formation after Treatment of Congenital form of Boutonniere Finger

2020 ◽  
Vol 53 (03) ◽  
pp. 455-456
Author(s):  
Hossein Akbari ◽  
Ali Foroutan ◽  
Peyman Akbari ◽  
Alireza Sherafat ◽  
Sayyed Abouzar Hosseini
Keyword(s):  
Congenital Form ◽  
Keloid Formation

Cerulean Cataract in a Person with Down s Syndrome

2021 ◽  
Vol 5 (2) ◽  
Author(s):  
Madbouhi K ◽  
◽  
Cherkaoui O ◽  
Keyword(s):  
Visual Acuity ◽  
Clinical Examination ◽  
Down's Syndrome ◽  
Anterior Segment ◽  
Down’S Syndrome ◽  
Congenital Form ◽  
The Right ◽  
Radial Arrangement ◽  
Loss Of Visual Acuity

We report the case of an 18-year-old patient who consults for a loss of visual acuity in the right eye for 1 year. On clinical examination, visual acuity is 20/100. Eye tone is 12 mmhg. Examination of the anterior segment shows the existence of a cataract made up of whitish opacities corresponding to a congenital cerulean cataract (Figure 1). The treatment consisted of a cataract cure by phacoemulsification with good progress. Cerulean cataract is a rare congenital form of bluish tint, made up of whitish opacities in concentric layers with a radial arrangement at their center. Visual acuity is fairly good in childhood but may deteriorate later. In the literature, the incidence of cataracts in Down’s children ranges from 5% to 50%. In previous studies of congenital or infantile cataract, 3-5 % of cases were associated with Down’s syndrome [1].

Congenital Clubfoot

PEDIATRICS ◽  
1966 ◽  
Vol 38 (3) ◽  
pp. 531-531
Author(s):  
PAUL P. GRIFFIN
Keyword(s):  
Club Foot ◽  
Review Of The Literature ◽  
Congenital Clubfoot ◽  
Excellent Review ◽  
Congenital Form ◽  
Principles Of Treatment ◽  
Physical Findings ◽  
Degrees Of Severity ◽  
Illustrated Book

In this short, well written and illustrated book the author gives an excellent review of the literature related to the etiology and pathology of the congenital form of clubfoot. In the first part of the book he clearly describes the physical findings one would see in clubfeet of varying degrees of severity. The remainder of the book is devoted to techniques and principles of treatment, several of which are only of historical interest. Doctor Hauser describes a method for the treatment of congenital club-foot which in his hands has given uniformly excellent results over a period of 23 years

scholarly journals Extension of the phenotypic spectrum of GLE1 ‐related disorders to a mild congenital form resembling congenital myopathy

2020 ◽  
Vol 8 (8) ◽  
Author(s):  
Mathieu Cerino ◽  
Chloé Di Meglio ◽  
Francesca Albertini ◽  
Frédérique Audic ◽  
Florence Riccardi ◽  
...  
Keyword(s):  
Congenital Myopathy ◽  
Congenital Form ◽  
Phenotypic Spectrum

Restoration of the Central Slip in Congenital Form of Boutonniere Deformity: Case Report

2014 ◽  
Vol 39 (10) ◽  
pp. 1978-1981 ◽  
Author(s):  
Jong-Pil Kim ◽  
Jai-Hyang Go ◽  
Chang-Hwan Hwang ◽  
Won-Jeong Shin
Keyword(s):  
Case Report ◽  
Congenital Form ◽  
Boutonniere Deformity ◽  
Central Slip ◽  
Boutonnière Deformity

Congenital form of spinal muscular atrophy predominantly affecting the lower limbs: a clinical and muscle MRI study

2004 ◽  
Vol 14 (2) ◽  
pp. 125-129 ◽  
Author(s):  
E. Mercuri ◽  
S. Messina ◽  
M. Kinali ◽  
C. Cini ◽  
C. Longman ◽  
...  
Keyword(s):  
Spinal Muscular Atrophy ◽  
Muscular Atrophy ◽  
Lower Limbs ◽  
Muscle Mri ◽  
Congenital Form ◽  
Mri Study

Inner ear pathology in osteogenesis imperfecta congenita

1980 ◽  
Vol 94 (7) ◽  
pp. 697-705 ◽  
Author(s):  
Makoto Igarashi ◽  
Austin I. King ◽  
C. Willy Schwenzfeier ◽  
Tsuneo Watanabe ◽  
Bobby R. Alford
Keyword(s):  
Osteogenesis Imperfecta ◽  
Inner Ear ◽  
Temporal Bone ◽  
Middle Ear ◽  
Stria Vascularis ◽  
Bony Labyrinth ◽  
Congenital Form ◽  
Basal Zone ◽  
Ear Ossicles ◽  
Osteogenesis Imperfecta Congenita

AbstractThis temporal bone report describes the inner ear deformities which were found in addition to the bony pathology in a case of osteogenesis imperfecta congenita. The labyrinthine pathology includes anomalously positioned and enlarged vestibular spaces, the existence of a scala communis (on one side) and the existence of hematoxylin dark-stained material in the basal zone of the stria vascularis.The appearance of temporal bone reports of osteogenesis imperfecta congenita is sporadic. Friedmann (1974)described changes in the bony capsule in one case of osteogenesis imperfecta congenita Zajtchul and Lindsay(1975)reported three cases of the congenital form of osteogenesis imperfecta with their temporal bone findings. Within recent years, Altmann reported three cases in 1962, Bretlau and Jorgensen reported one case in 1969, Bergstrom and others reported one case in 1972, and Bergstrom described the temporal bone findings in four infants in 1977. The pathologic description of the temporal bone in osteogenesis imperfecta congenita has been focused more or less on the structures of the bony labyrinth and the middle ear ossicles, with a brief description of the inner ear. In this report, we describe anomalous inner ear structures in osteogenesis imperfecta congenita.

scholarly journals Will New Approaches in The Treatment of Supraventricular Tachycardia Affect The Cardiologists’ Perspective?

2019 ◽  
Vol 2 (2) ◽  
pp. 01-01
Author(s):  
Cetin Sanlialp Sara
Keyword(s):  
Cardiac Surgery ◽  
Supraventricular Tachycardia ◽  
Postoperative Period ◽  
Common Type ◽  
Supraventricular Arrhythmias ◽  
Junctional Ectopic Tachycardia ◽  
Congenital Cardiac Surgery ◽  
Congenital Form ◽  
New Approaches

Junctional ectopic tachycardia(JET) is one of the rare supraventricular arrhythmias(1). JET is categorized by two types. The less common type of JET is congenital form and the more common type has been seen in postoperative period of congenital cardiac surgery

Null mutations and lethal congenital form of glycogen storage disease type IV

2007 ◽  
Vol 361 (2) ◽  
pp. 445-450 ◽  
Author(s):  
Stefania Assereto ◽  
Otto P. van Diggelen ◽  
Luisa Diogo ◽  
Eva Morava ◽  
Denise Cassandrini ◽  
...  
Keyword(s):  
Glycogen Storage Disease ◽  
Storage Disease ◽  
Glycogen Storage Disease Type ◽  
Glycogen Storage ◽  
Disease Type ◽  
Congenital Form ◽  
Type Iv
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