Juvenile glaucoma in a child with caudal regression syndrome
نویسندگان
چکیده
منابع مشابه
Infantile glaucoma and punctal atresia in a child with caudal regression syndrome.
C audal regression syndrome (CRS) is a rare embryopathy characterized by maldevelopment of the vertebrae, visceral organs, and lower extremities. Patients with CRS have deformities of the sacrococcygeal vertebrae and develop neurogenic bladder from dysfunction of the sacral nerve root. Additional anomalies include congenital heart defects, intestinal malrotation, agenesis of the genitourinary s...
متن کاملCaudal Regression Syndrome
Caudal regression syndrome (CRS) is a rare neural tube defect affecting terminal spinal segments and cord manifesting as neurological deficit ranging from bladder and bowel involvement to severe sensory motor deficits in lower limbs. It has sporadic appearance and maternal diabetes, genetic factors, teratogens and hypoperfusion are considered as possible etiologic factors and it can be associat...
متن کاملCaudal regression syndrome.
INTRODUCTION The regression caudal syndrome includes a spectrum of malformations which vary from the symptomless coccygeal agenesis until thoracic vertebrae and sacrococcygeal agenesis with severe neurological deficit; it is associated sometimes with malformations in other organs and systems. We present a case of partial agenesis of sacro and coccix with neuromuscular, sphincter and orthopedist...
متن کاملPrenatal diagnosed caudal regression syndrome
Background: Caudal regression syndrome (CRS) is a rare complex congenital anomaly which is characterized by agenesis of the sacral and lumbar spine. Pelvis, lower extremity, genitourinary, cardiac anomalies and lower extremity neurological and motor development deficits may be accompanied. The exact etiology is unclear but the maternal insulin-dependent diabetes mellitus (hyperglycaemia during ...
متن کاملDistal Innervation in a Child Affected from a 3 Syndrome of Caudal Regression
Caudal regression syndrome (CRS) is a congenital abnormality characterized by an 17 incomplete development of the spinal cord (SC) and other abnormalities. We studied a 9-months 18 old CRS child presenting: interruption of SC at L2-L3 level, sacral agenesis, lack of innervation of 19 the inferior limbs (flaccid paraplegia) and neurogenic bladder and bowel. Given the effects of 20 growth hormone...
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ژورنال
عنوان ژورنال: Acta Ophthalmologica
سال: 2010
ISSN: 1755-375X
DOI: 10.1111/j.1755-3768.2010.01999.x