A Type 3 Klippel Feil Syndrome Case With Atrial Septal Defect and Atrial Septal Aneurysm

Abstract

Klippel Feil syndrome (KFS) is a rare congenital disorder characterized by short neck due to abnormal fusion of cervical vertebrae, limited head and neck motion and low posterior hairline. We present a rare case of type 3 KFS with the fusion of cervical and thoracic vertebrae, cervical hemivertebrae anomaly, Sprengel’s deformity, rib fusion anomaly, accompanied by atrial septal defect/septal aneurysm, thereby reviewing the literature about this syndrome.

Authors and Affiliations

Aysu Türkmen Karaağaç

Keywords

Related Articles

Neonatal Alloimmune Thrombocytopenia

Neonatal alloimmune thrombocytopenia is the most common cause of immune-mediated thrombocytopenia in the newborn period. The disorder results from placental transfer of maternal alloantibodies directed against paternally...

Cardiometabolic Risk Profile and its Relation with the Waist Circumference to Height Ratio in Turkish School-Age Children

Background: Obesity, cardiovascular diseases and diabetes have been rapidly increasing in pediatric age group all around the world. Therefore, cardiometabolic risk factors (CMRF) should be carefully screened beginning fr...

A Yellow and Benign Tumor in a Newborn

The sebaceous hamartoma of Jadassohn (HSJ) is a congenital malformation most often discovered during infancy. Early surgical excision is motivated by the rare risk of malignant tumor development, especially basal cell ca...

The Management of Hereditary Epidermolysis Bullosa: Experience of a Moroccan Sub-Population

Hereditary epidermolysis bullosa (EBH) is a heterogeneous group of rare genodermatoses, characterized by cutaneous or mucosal fragility, localized or generalized. These are diseases of varying severity, which can have a...

A Type 3 Klippel Feil Syndrome Case With Atrial Septal Defect and Atrial Septal Aneurysm

Klippel Feil syndrome (KFS) is a rare congenital disorder characterized by short neck due to abnormal fusion of cervical vertebrae, limited head and neck motion and low posterior hairline. We present a rare case of type...

Download PDF file
  • EP ID EP212900
  • DOI 10.19070/2572-7354-160005
  • Views 131
  • Downloads 0

How To Cite

Aysu Türkmen Karaağaç (2016). A Type 3 Klippel Feil Syndrome Case With Atrial Septal Defect and Atrial Septal Aneurysm. International Journal of Pediatric Health Care & Advancements (IJPA), 3(1), 13-16. https://europub.co.uk/articles/-A-212900