SavedAdd your journal

Journals / Abant Tıp Dergisi / 2021 / Cilt: 10 Sayı: 3

Dandy-Walker Malformation With Postaxial Polydactyly: Newborn Case Report

Dandy-Walker Malformasyonu İle Postaksiyel Polidaktili Birlikteliği: Yenidoğan Olgu Sunumu

Mustafa Özdemir(CUKUROVA UNIVERSITY, FACULTY OF MEDICINE)0000-0001-5644-8283
Tugay Tepe(CUKUROVA UNIVERSITY, FACULTY OF MEDICINE)0000-0002-7926-8442
Şerif Hamitoğlu(CUKUROVA UNIVERSITY, FACULTY OF MEDICINE)0000-0002-9904-3427
Ahmet İbrahim Kurtoğlu(CUKUROVA UNIVERSITY, FACULTY OF MEDICINE)0000-0001-8581-5652
Ferda Özlü(CUKUROVA UNIVERSITY, FACULTY OF MEDICINE)0000-0002-2092-8426
Hacer Yapıcıoğlu(CUKUROVA UNIVERSITY, FACULTY OF MEDICINE)0000-0001-6295-553X
Pages
401–404
Publication Date
2021-12-21
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Here, we present an infant with postaxial polydactyl accompanying Dandy-Walker malformation because of rare.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Dandy-Walker malformation is a rare congenital malformation, characterized by agenesis or hypoplasia of the cerebellar vermis, cystic dilatation of the 4th ventricle and enlargement of the posterior fossa.
📊
Key Findings & Data:Postnatal hydrocephalus develops in approximately 70-90% of the patients.
💡
Conclusion & Impact:Here, we present an infant with postaxial polydactyl accompanying Dandy-Walker malformation because of rare.
🔬Design:Olgu Sunumu
📍Scope:Comprehensive Sample
⚙️Variables:Dandy-Walker malformasyonu · Polidaktili · Hidrosefali

Abstract

Dandy-Walker malformation is a rare congenital malformation, characterized by agenesis or hypoplasia of the cerebellar vermis, cystic dilatation of the 4th ventricle and enlargement of the posterior fossa. Postnatal hydrocephalus develops in approximately 70-90% of the patients. The relationship of Dandy-Walker malformation with postaxial polydactyl has been defined as a possible autosomal recessive syndrome (OMIM 220220). Here, we present an infant with postaxial polydactyl accompanying Dandy-Walker malformation because of rare.

Özet

Dandy-Walker malformasyonu, serebellar vermis agenezisi veya hipoplazisi, 4. ventrikülün kistik dilatasyonu ve posterior fossa genişlemesi ile karakterize nadir bir konjenital malformasyondur. Hastaların yaklaşık %70-90’ında postnatal hidrosefali gelişir. Dandy-Walker malformasyonun postaksiyel polidaktili ile ilişkisi ise, olası bir otozomal resesif sendrom (OMIM 220220) olarak tanımlanmıştır. Bu vakada Dandy-Walker malformasyonu tanısı alan ve postaksiyel polidaktilisi olan bir infant nadir olması nedeniyle sunuldu.

🔖

Cite This Article

Özdemir, M., Tepe, T., Hamitoğlu, Ş., Kurtoğlu, A. İ., Özlü, F., Yapıcıoğlu, H. (2021). Dandy-Walker Malformation With Postaxial Polydactyly: Newborn Case Report. Abant Tıp Dergisi, Cilt: 10 Sayı: 3, 401–404. https://doi.org/10.47493/abantmedj.950391

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (12)

  1. Forzano F, Mansour S, Ierullo A, Homfray T, Thilaganathan B. Posterior fossa malformation in fetuses: A report of 56 further cases and a review of the literature [Internet]. Vol. 27, Prenatal Diagnosis. Prenat Diagn; 2007 [cited 2021 Mar 24]. p. 495–501. Available from: https://pubmed.ncbi.nlm.nih.gov/17367101/
  2. Kumar R, Jain MK, Chhabra DK. Dandy-Walker syndrome: Different modalities of treatment and outcome in 42 cases. Child’s Nerv Syst [Internet]. 2001 May [cited 2021 Mar 24];17(6):348–52. Available from: https://pubmed.ncbi.nlm.nih.gov/11417415/
  3. Zimmerman RA, Bilaniuk LT. Magnetic resonance evaluation of fetal ventriculomegaly-associated congenital malformations and lesions [Internet]. Vol. 10, Seminars in Fetal and Neonatal Medicine. W.B. Saunders Ltd; 2005 [cited 2021 Mar 24]. p. 429–43. Available from: https://pubmed.ncbi.nlm.nih.gov/15964253/
  4. Osenbach RK, Menezes AH. Diagnosis and management of the dandy-walker malformation: 30 years of experience. Pediatr Neurosurg [Internet]. 1992 [cited 2021 Mar 24];18(4):179–89. Available from: https://pubmed.ncbi.nlm.nih.gov/1472430/
  5. Scher MS, Belfar H, Martin J, Painter MJ. Destructive Brain Lesions of Presumed Fetal Onset: Antepartum Causes of Cerebral Palsy. Pediatrics. 1991;88(5).
  6. Ten Donkelaar HJ, Lammens M, Wesseling P, Thijssen HOM, Renier WO. Development and developmental disorders of the human cerebellum [Internet]. Vol. 250, Journal of Neurology. J Neurol; 2003 [cited 2021 Mar 24]. p. 1025–36. Available from: https://pubmed.ncbi.nlm.nih.gov/14504962/
  7. Sawaya R, McLaurin RL. Dandy-Walker syndrome. Clinical analysis of 23 cases. J Neurosurg [Internet]. 1981 [cited 2021 Mar 24];55(1):89–98. Available from: https://pubmed.ncbi.nlm.nih.gov/6972441/
  8. Krieger AJ, Detwiler J, Trooskin S. Respiration in an infant with the Dandy-Walker syndrome. Neurology [Internet]. 1974 [cited 2021 Mar 24];24(11):1064–7. Available from: https://pubmed.ncbi.nlm.nih.gov/4472854/
  9. Gurrieri F, Franco B, Toriello H, Neri G. Oral-facial-digital syndromes: Review and diagnostic guidelines. In: American Journal of Medical Genetics, Part A [Internet]. Am J Med Genet A; 2007 [cited 2021 Mar 24]. p. 3314–23. Available from: https://pubmed.ncbi.nlm.nih.gov/17963220/
  10. Kosaki K, Curry CJ, Roeder E, Jones KL. Ritscher-Schinzel (3C) syndrome: Documentation of the phenotype. Am J Med Genet [Internet]. 1997 Feb 11 [cited 2021 Mar 24];68(4):421–7. Available from: https://pubmed.ncbi.nlm.nih.gov/9021015/
  11. Cohen MM. Perspectives on asymmetry: The Erickson lecture [Internet]. Vol. 158 A, American Journal of Medical Genetics, Part A. Wiley-Liss Inc.; 2012 [cited 2021 Mar 24]. p. 2981–98. Available from: https://pubmed.ncbi.nlm.nih.gov/23132826/
  12. Brancati F, Dallapiccola B, Valente EM. Joubert Syndrome and related disorders [Internet]. Vol. 5, Orphanet Journal of Rare Diseases. Orphanet J Rare Dis; 2010 [cited 2021 Mar 24]. Available from: https://pubmed.ncbi.nlm.nih.gov/20615230/