Journal Basic Info

  • Impact Factor: 1.809**
  • H-Index: 6
  • ISSN: 2474-1655
  • DOI: 10.25107/2474-1655
**Impact Factor calculated based on Google Scholar Citations. Please contact us for any more details.

Major Scope

  •  Child Birth
  •  Hepatitis
  •  Pathology
  •  Lung Cancer
  •  Orthopedics & Rheumatology
  •  Cardio-Thoracic Surgery
  •  Hepatology
  •  Asthma

Abstract

Citation: Ann Clin Case Rep. 2017;2(1):1230.DOI: 10.25107/2474-1655.1230

Prenatal Diagnosis of Achondrogenesis Type 2 in the Early Second Trimester by using Three-Dimensional Computed Tomography

Kana Sugeta, Shunichiro Tsuji, Daisuke Katsura, Fuminori Kimura, Ayumi Seko-Nitta and Takashi Murakami

1Department of Obstetrics and Gynecology, Shiga University of Medical Science Seta Tsukinowa-cho, Japan 2Department of Radiology, Shiga University of Medical Science, Seta Tsukinowa-cho, Japan

*Correspondance to: Shunichiro Tsuji 

 PDF  Full Text Case Report | Open Access

Abstract:

Achondrogenesis type 2 (ACG2) is a lethal skeletal disorder that is characterized by extremely short limbs with cupped and splayed metaphyses and poor vertebral body ossification. A 23-year-old Japanese woman (gravida 1, para 0) was referred to our hospital at 19 weeks and 0 days gestation with the fetus having severe shortening of the long bones. According to ultrasonographic examination, thanatophoric dysplasia type 1 or ACG2 was suspected. Therefore, we performed three-dimensional computed tomography (3D-CT) which showed the lack of ossification of the fetal vertebral bodies clearly. We diagnosed ACG2, and the parents decided on termination of the pregnancy. Here we report a case of ACG2 that was clearly identified with 3D-CT in the early second trimester.

Keywords:

Achondrogenesis; Prenatal diagnosis; Three-dimensional computed tomography

Cite the Article:

Sugeta K, Tsuji S, Katsura D, Kimura F, Seko-Nitta A, Murakami T. Prenatal Diagnosis of Achondrogenesis Type 2 in the Early Second Trimester by using Three-Dimensional Computed Tomography. Ann Clin Case Rep. 2017; 2: 1230.

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