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Journals / Jinekoloji-Obstetrik ve Neonatoloji Tıp Dergisi / 2016 / Cilt: 13 - Sayı: 3

A Case Of Pena-Shokeir Syndrome

Pena-Shokeir Sendromu

Nurdan URAS
Evrim Alyamaç DİZDAR
Turan DERME
Halit HALİL
Şerife Suna OĞUZ
Pages
135–136
Publication Date
2022-10-18
DOI
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AI Summary & Key Takeaways

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

Physical examination showed multiple congenital anormalies congruent with features of Pena-Shokeir syndrome.

📌 3 Key Takeaways

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Objective & Hypothesis:Pena-Shokeir syndrome is characterised by fetal akinesia, intrauterine growth retardation, deformites of musculoskeletal system, facial anomalies, pulmonary hypoplasia, short umbilical cord and polyhydramnios.
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Key Findings & Data:In this manuscript we reported a newborn case born at the 35th gestational weeks whose prenatal ultrasonography showed reduced fetal movements and multiple deformities of extremities.
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Conclusion & Impact:Physical examination showed multiple congenital anormalies congruent with features of Pena-Shokeir syndrome.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Pena-Shokeir sendrom · multipl konjenital anomaliler · Pena Shokeir syndrome

Abstract

Pena-Shokeir syndrome is characterised by fetal akinesia, intrauterine growth retardation, deformites of musculoskeletal system, facial anomalies, pulmonary hypoplasia, short umbilical cord and polyhydramnios. In this manuscript we reported a newborn case born at the 35th gestational weeks whose prenatal ultrasonography showed reduced fetal movements and multiple deformities of extremities. Physical examination showed multiple congenital anormalies congruent with features of Pena-Shokeir syndrome.

Özet

Pena-Shokeir sendromu fetal akinezi, intrauterin gelişme geriliği, kas ve iskelet deformiteleri, fasiyal anomaliler, pulmoner hipoplazi, kısa umbilikal kord, polihidramniyos ile giden klinik bir fenotipdir. Bu makalede 35 haftalık doğan, prenatal ultrasonografisinde fetal hareketleri yavaş ve ekstremitelerinde deformite olan, postnatal muayenesinde multipl konjenital anomali tespit edilen Pena-Shokeir sendromu özellikleri gösteren bir vaka sunulmuştur.

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Cite This Article

URAS, N., DİZDAR, E. A., DERME, T., HALİL, H., OĞUZ, Ş. S. (2022). A Case Of Pena-Shokeir Syndrome. Jinekoloji-Obstetrik ve Neonatoloji Tıp Dergisi, Cilt: 13 - Sayı: 3, 135–136. https://ajindex.com/articles/558776

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References (3)

  1. Pena SD, Shokeir MH. Syndrome of camptodactyly, multiple ankyloses, facial anomalies and pulmonary hypoplasia. A lethal condition. J Pediatr 1974; 85: 373–5. Herring JA. Orthopedics related syndromes. In: Tachdjian’s Pediatric Ort- hopedics. Herring JA (ed). 5’th edition. ELSEVER. 2013; 2: P541-547. Shivaprakash.N.C, Uday Shankar and Kedarnath.G.T. Pena-Shokeir Sy- ndrome: A Case Report. BMR Medicine 2014; 1: 1-4.
  2. Santana EFM, Serni PNO, Rolo LC, and Jşnior EA. Prenatal Diagno- sis of Arthrogryposis as a Phenotype of Pena-Shokeir Syndrome using Two- and Three-dimensional Ultrasonography. J Clin Imaging Sci. 2014; 4: 20. Şenocak EU, Oğuz KK, Haliloğlu G, Karcaaltıncaba A, Akata D and Kande- mir ö. Prenatal diagnosis of Pena-Shokeir syndrome phenotype by ultra- sonography and MR imaging. Pediatr Radiol 2009; 39:377-380. Jones KJ. Pena Shokier phenotype. In: Jones KJ (eds). Smith’s recogni- zable pattern of human malformations. 5th ed. Philadelphia: W. B. Saun- ders Co; 1999. 174–175. Hall JG; Arthrogryposis multiplex congenita: etiology,genetics, classifi- cation, diagnostic approach, and general aspects. J Pediatr Orthop B. 1997;6(3):159-66.
  3. Çalık M, Çakmak A, Soran M, Ataş A. Farklı Anomalilerin Eşlik Ettiği Potter Sendromu: Vaka Sunumu Tıp Araştırmaları Dergisi: 2008: 6:121 -124