Characterization of ultrasound and postnatal pathology in fetuses with heterotaxy syndrome [PDF]
BackgroundTo explore the diagnostic clues and abnormality spectrum of heterotaxy syndrome by prenatal ultrasonography and postnatal verification.MethodsThe prenatal ultrasonic data of 88 heterotaxy syndrome fetuses were analyzed retrospectively as left ...
Qiumei Wu +11 more
doaj +4 more sources
Heterotaxy Syndrome with Polysplenia, Fused Adrenal Glands, and Diabetes Mellitus [PDF]
Heterotaxy syndrome is a rare congenital heart disease with a disarrangement of the heart and abdominal organs. We present a young African female with features of heart failure, diffuse irregular cardiac murmurs, and palpable, tender epigastric mass.
Abid M Sadiq, Adnan M Sadiq
doaj +2 more sources
Pheochromocytoma in a patient with heterotaxy syndrome: a case report [PDF]
Background Heterotaxy syndrome is a rare congenital condition characterized by abnormal arrangement of thoracoabdominal organs, often associated with complex cardiac and splenic anomalies. Pheochromocytoma is a rare neuroendocrine tumor that overproduces
Farid Farahani Rad +3 more
doaj +2 more sources
A Rare Variation of the Heterotaxy Syndrome [PDF]
Heterotaxy syndrome is a rare, complex, and confusing type of the situs anomalies. It is not possible to estimate the degree of lateralization, isomerism, and rotational variation in these types of cases.
Alper Dilli +4 more
doaj +3 more sources
Cardiac surgical outcomes of patients with heterotaxy syndromeCentral MessagePerspective [PDF]
Objectives: The study objectives were to analyze the outcomes of pediatric patients with heterotaxy syndrome undergoing cardiovascular surgery and to determine the predictors of mortality.
Manan H. Desai, MD +10 more
doaj +2 more sources
Heterotaxy Syndrome: Discordant Growth. [PDF]
Heterotaxy syndrome implies a discordance between placement of thoracic organs with respect to abdominal organs. A large number of these have associated congenital heart defects. This syndrome is unique as every patient is different and can have any permutation and combination of symptoms.
Yadav P +3 more
europepmc +4 more sources
Heterotaxy syndrome with complex congenital heart disease, facial palsy, and asplenia: A rare newborn finding [PDF]
Heterotaxy syndrome is associated with asplenia/polysplenia and complex congenital heart disease. Facial palsy in heterotaxy is very rare. The management is still challenging with a poor prognosis. Proper counseling to the family about the disease course,
Sanjeev Kharel +6 more
doaj +2 more sources
Heterotaxy syndrome – An unusual cause for bowel obstruction in an adult [PDF]
Heterotaxy syndrome, also known as situs ambiguous, is a spectrum of pathology due to loss of the normal right-to-left asymmetry of the thoraco-abdominal organs.
Radhiya Minty, Tanaka Gomba, Rabia Abid
doaj +2 more sources
Locally invasive cholangiocarcinoma causing gastric outlet obstruction in heterotaxy syndrome: A case report and review of literature [PDF]
Heterotaxy syndrome is a disease of embryo development resulting in abnormal distribution of thoracic and abdominal organs across the left-right axis.
Wanyang Qian, MD +3 more
doaj +2 more sources
Heterotaxy syndrome with complex single-ventricle physiology and left-sided Bochdalek hernia: Multisystem characterization by cardiothoracic CT [PDF]
Heterotaxy syndrome comprises a spectrum of laterality defects frequently associated with complex congenital heart disease and extracardiac anomalies. We report a 2-year-old male who presented with persistent cyanosis, recurrent respiratory infections ...
Aamir M. Kanji, MD, MMed +3 more
doaj +2 more sources

