Caffey Award

نویسندگان

  • D. S. Babcock
  • B. K. Han
چکیده

Children with meningomyeloceles have problems involving several organ systems and often require repeated radiologic examinations. They have multiple cranial defects, particularly the Arnold-Chiari II malformation and associated hydrocephalus. Cranial sonographic findings in 29 patients included hydrocephalus with pointing of the frontal horns, asymmetry of the lateral ventricles, and relative enlargement of the occipital horns compared with the frontal horns. Partial absence of the septum pellucidum, abnormalities of the third ventricle including a prominent massa intermedia, prominent anterior commissure, and prominent suprapineal recess were also seen. A V-shaped tentorium cerebelli was demonstrated on axial scan as well as low position of the tent on coronal scan. The posterior fossa pseudomass was demonstrated. A prominent interhemispheric fissure was also seen in some patients. Sonography is an excellent method for following ventricular size and shunt function since repeated examinations can readily be performed.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

COL1A1 gene

A particular mutation in the COL1A1 gene causes infantile cortical hyperostosis, commonly known as Caffey disease. The signs and symptoms of Caffey disease are usually apparent by the time an infant is 5 months old. This condition is characterized by swelling of soft tissues (muscles, for example), pain, and excessive new bone formation (hyperostosis). The bone abnormalities mainly affect the j...

متن کامل

Kenny-Caffey syndrome. Case report and literature review.

Kenny-Caffey Syndrome is a rare syndrome characterized by growth retardation, uniformly small slender long bones with medullary stenosis, thickened cortex of the long bones, hypocalcemia possibly with tetany at an early age, hyperphosphatemia, ocular abnormalities, and normal intelligence. We report a child with Kenny-Caffey Syndrome and idiopathic hypoparathyroidism and present a review of the...

متن کامل

Prenatal Caffey Disease Case Report and Review of the Literature

Background: Two forms of Caffey disease or cortical hyperostosis were described, a severe prenatal form and a milder infantile one. Both are characterized by massive periosteal bone formation that typically involve the diaphyses of long bones. Case Report: We report a 26 week +4 days old baby girl whose mother had severe polyhydramnios. The baby was born with hydrops fetalis and some dysmorphic...

متن کامل

Infantile cortical hyperostosis (Caffey disease): a possible misdiagnosis as physical abuse.

Infantile cortical hyperostosis (Caffey disease) is a rare self-limiting inflammatory bony disease of early infancy. We report a 1-month-old Chinese boy with Caffey disease who presented with painful swelling over his shins bilaterally. Physical abuse was initially suspected, but the radiological findings of periosteal thickening over multiple bones (particularly the mandible), symmetrical invo...

متن کامل

SQUIRES RECEIVES OUTSTANDING ACHIEVEMENT AWARD FOR STEWARDSHIP

Dr. Victor R. Squires of Adelaide, Australia received the Outstanding Achievement Award for Stewardship at the Society for Range Management’s 68th Annual Meeting held in Sacramento, California earlier this month. The Outstanding Achievement Award is presented by the Society for Range Management for outstanding achievement to members and other qualified individuals and groups working with rangel...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2013