Journals / Turkish Journal of Obstetrics and Gynecology / 2019 / Cilt: 16 - Sayı: 3

Fetal fibular hemimelia with focal femoral deficiency: A case report

Pages
205–207
DOI
—
🏛️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)

Long bone shortness can be a part of syndrome or an isolated finding.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Fibular hemimelia (FH) is a congenital deficiency in which a part or all of the fibular bone is hypoplastic or aplastic and associated with hypoplastic tibia and foot anomalies.
📊
Key Findings & Data:We report a case of unilateral FH with focal femoral deficiency detected at 18 weeks of gestation during a routine ultrasonographic anatomic screening.
💡
Conclusion & Impact:Long bone shortness can be a part of syndrome or an isolated finding.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

Fibular hemimelia (FH) is a congenital deficiency in which a part or all of the fibular bone is hypoplastic or aplastic and associated with hypoplastic tibia and foot anomalies. The main differential diagnoses include proximal focal femoral dysplasia, Femur-Fibula-Ulna syndrome, and Femoral Hypoplasia-Unusual Facies syndrome. Proximal focal femoral dysplasia, which has a short, angulated femur with normal mineralization may be associated with FH. We report a case of unilateral FH with focal femoral deficiency detected at 18 weeks of gestation during a routine ultrasonographic anatomic screening. Sonographic findings were a unilateral short femur (1.8 cm, 3 weeks shorter than expected for gestational weeks), agenesis of ipsilateral fibula and angulation of ipsilateral tibial shaft. During a routine ultrasonographic anatomic scan, all the long bones are carefully measured and evaluated. Long bone shortness can be a part of syndrome or an isolated finding.

🔖

Cite This Article

YAKIŞTIRAN, B., ALTINBOĞA, O., YÜCE, T., ÇAĞLAR, A. T. (2019). Fetal fibular hemimelia with focal femoral deficiency: A case report. Turkish Journal of Obstetrics and Gynecology, Cilt: 16 - Sayı: 3, 205–207. https://ajindex.com/articles/376402

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (8)

  1. Tsai A, Kleinman PK, Laor T, Kasser JR. Lower-extremity growth patterns and skeletal maturation in children with unilateral fibular hemimelia. Pediatr Radiol 2019;49:122-7
  2. Monteagudo A, Dong R, Timor-Tritsch IE. Fetal fibular hemimelia: case report and review of the literature. J Ultrasound Med 2006;25:533-7
  3. Achterman C, Kalamchi A. Congenital deficiency of the fibula. J Bone Joint Surg Br 1979;61-B:133-7
  4. Filly AL, Robnett-Filly B, Filly RA. Syndromes with focal femoral deficiency: strengths and weaknesses of prenatal sonography. J Ultrasound Med 2004;23:1511-6
  5. Cullier F, Cartault F, Lemaire P. Absence of fibula, type II. www.fetus.net 2004-03-25-14
  6. Pallavee P, Samal R, Begum J, Ghose S. Foetal fibular hemimelia with focal femoral deficiency following prenatal misoprostol use: a case report. J Obstet Gynaecol 2016;36:760-1
  7. Wilcox WR, Coulter CP, Schmitz ML. Congenital limb deficieny disorders. Clin Perinatol 2015;42:281-300 8. Shawky R, Elkhalek H, Gad S, Mohammad SA. Unilateral proximal focal femoral deficiency, fibular aplasia, tibial campomelia and oligosyndactyly in an Egyptian child: Probable FFU syndrome. Egyptian Journal of Medical Human Genetics 2014;15:299-303
  8. Popkov A, Aranovich A, Popkov D. Prevention of recurrence of tibia and ankle deformities after bone lenghtening in children with type 2 fibular hemimelia. Int Orthop 2015;39:1365-70.