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Congenital bilateral
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Brain arteriovenous malformations (AVMs) are rare congenital developmental vascular lesions, and often presents with symptoms upon rupture. The controversy exists as to whether pregnancy confers an increased risk of intracranial hemorrhage. The diagnosis of brain AVMs, in the absence of brain imaging, is challenging in resource-limited settings, particularly in sub-Saharan Africa.
7p
vitiki
30-01-2024
6
2
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Transverse congenital limb deficiency is a common limb deficiency where there is normal limb development until a certain point, beyond which no anatomical structure exists. Typically, this presents as an isolated and spontaneous abnormality as a result of arrest during limb bud development.
6p
vigamora
23-05-2023
2
2
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Part 1 of ebook "Obstetric imaging: Fetal diagnosis and care" provide readers with content about: atlas of selected normal images; thorax; congenital cystic adenomatoid malformation of the lung; bronchopulmonary sequestration; scimitar syndrome; retroperitoneum; abnormal kidney location; abnormal kidney size; bilateral renal agenesis; unilateral renal agenesis; duplicated collecting system; multicystic dysplastic kidney;...
441p
duonghoanglacnhi
07-11-2022
21
7
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The domestic chinchilla has been descended from Chinchilla lanigera (long-tailed Chinchilla) or Chinchilla chinchilla (short-tailed Chinchilla). Both species of chinchilla are currently listed as endangered by the IUCN Red List of Threatened Species. Over the past 20 years, they have spread as pets and overall knowledge about their care is improving. The present case report describes a congenital diaphragmatic hernia in a Chinchilla lanigera.
5p
vidarwin
22-02-2022
14
1
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The aim of this study was to determine whether computer-aided training (CAT) of motor tasks would increase muscle activity and change its spatial distribution in a patient with a bilateral upper-limb congenital transverse deficiency.
13p
vimariana2711
22-12-2020
4
0
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Arthrogryposis is a common inherited deformity characterized by contracture of tendons and fixation of joints. In the present case, a pluriparous buffalo was presented in the clinics with the history of straining from 12 hours. After performing the caesarean section, a dead male buffalo calf was delivered with bilateral arthrogryposis of carpel joint and fetlock joint in both the forelimb and fetlock joint in both the hind limb.
3p
chauchaungayxua8
03-10-2020
9
2
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Prune belly syndrome is a rare congenital malformation of unknown aetiology and is characterised by abnormalities of the urinary tract, a deficiency of abdominal musculature and bilateral cryptorchidism in males.
6p
vivalanbo2711
19-03-2020
16
2
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LAMB2 mutations cause Pierson syndrome (OMIM 609049), an autosomal recessive genetic disease typically characterized by congenital nephrotic syndrome (CNS) and early onset renal failure, as well as bilateral microcoria.
7p
vichengna2711
25-02-2020
16
0
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Klippel-Trénaunay syndrome (KTS) is a rare congenital condition characterized by the clinical triad of capillary malformations (port wine stains), varicose veins with or without venous malformations, and bony and/or soft tissue hypertrophy.
4p
virome2711
13-01-2020
9
0
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Gillespie syndrome is a rare, congenital, neurological disorder characterized by the association of partial bilateral aniridia, non-progressive cerebellar ataxia and intellectual disability. Homozygous and heterozygous pathogenic variants of the ITPR1 gene encoding an inositol 1, 4, 5- triphosphate- responsive calcium channel have been identified in 13 patients recently.
5p
vidublin2711
13-01-2020
14
0
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Congenital bilateral vocal cord paralysis is a rare occurrence. Approximately half the cases are associated with a major comorbidity, usually neurological, neuromuscular or malformative.
6p
vidublin2711
13-01-2020
11
0
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Congenital Anomalies of the Lumbar Spine Spondylolysis is a bony defect in the pars interarticularis (a segment near the junction of the pedicle with the lamina) of the vertebra; the etiology may be a stress fracture in a congenitally abnormal segment. The defect (usually bilateral) is best visualized on oblique projections in plain x-rays, CT scan, or single photon emission CT (SPECT) bone scan and occurs in the setting of a single injury, repeated minor injuries, or growth.
5p
ongxaemnumber1
29-11-2010
66
3
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