Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

238
Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

233
Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

DANDY-WALKER SYNDROME: A REVIEW OF NEW DIAGNOSIS AND MANAGEMENT IN CHILDREN

Pages

  47-52

Abstract

 Context: DANDY-WALKER SYNDROME (DWS) or MALFORMATION (DWM) characterizes a hereditary abnormality categorized via agenesis or hypoplasia of the cerebellar vermis, cystic dilation of the fourth ventricle, and expansion of the posterior fossa with or without hydrocephalus. This review aimed at describing the basic clinic pathologic features of DWS, its DIAGNOSIS by other central nervous system (CNS), systemic genetic relatives, and new treatment modalities.Evidence Acquisition: Training and publishing in this field is very limited. Among54 articles in this era, a total of in 31 articles were included in the current evaluation.Results: The etiology of DWSis uncertain, however, is supposed to be a consequence of the mixture of ecological and genetic causes. The most common postnatal appearance is macro crania. Additional signs and symptoms could include huge posterior fossa, sunset sign, seizures, spasticity, apnea, respiratory failure, delayed milestones, hydrocephalus, and increased intracranial pressure. Currently, DWS is diagnosed completely with anatomic definitions that can be recognized on ultrasound or Magnetic resonance imaging (MRI) and computed tomography (CT) intrauterine or postnatal.Conclusions: Dandy walker syndrome occurs as a comparatively rare origin of hydrocephalus and might go along with numerous inherited CNS and systemic anomalies. Even though it is usually treated for related hydrocephalus, the abnormality causes no detectable clinical syndrome. It is identified with antenatal or postnatal imaging via ultrasound, CT, or MRI. Hydrocephalus and the cyst in posterior fossa can be treated with surgery, via shunting processes, endoscopy, or both. Prognosis has enhanced meaningfully from the time of its original report; yet, it is typically dependent on the accompanying abnormalities.

Cites

  • No record.

    • References

    Cite

    APA: Copy

    HADDADI, KAVEH, ZARE, AMIRHOSSEIN, & ASADIAN, LEILA. (2018). DANDY-WALKER SYNDROME: A REVIEW OF NEW DIAGNOSIS AND MANAGEMENT IN CHILDREN. JOURNAL OF PEDIATRICS REVIEW, 6(2), 47-52. SID. https://sid.ir/paper/341207/en

    Vancouver: Copy

    HADDADI KAVEH, ZARE AMIRHOSSEIN, ASADIAN LEILA. DANDY-WALKER SYNDROME: A REVIEW OF NEW DIAGNOSIS AND MANAGEMENT IN CHILDREN. JOURNAL OF PEDIATRICS REVIEW[Internet]. 2018;6(2):47-52. Available from: https://sid.ir/paper/341207/en

    IEEE: Copy

    KAVEH HADDADI, AMIRHOSSEIN ZARE, and LEILA ASADIAN, “DANDY-WALKER SYNDROME: A REVIEW OF NEW DIAGNOSIS AND MANAGEMENT IN CHILDREN,” JOURNAL OF PEDIATRICS REVIEW, vol. 6, no. 2, pp. 47–52, 2018, [Online]. Available: https://sid.ir/paper/341207/en

    Related Journal Papers

  • No record.

    • Related Seminar Papers

  • No record.

    • Related Plans

  • No record.

    • Recommended Workshops






    Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button