Congenital Agenesis of the Pericardium

2021 ◽  
Author(s):  
Benjamin Collaer ◽  
Sayf Ayad Al-Katib, MD
Keyword(s):  
Congenital Agenesis

Mitral Valve Surgery in a Patient with Dextrocardia and 180° Counter-clockwise Rotated Heart Due to Congenital Agenesis of the Right Lung

2013 ◽  
Vol 28 (6) ◽  
pp. 635-637
Author(s):  
Yosuke Atsumi ◽  
Shigehiko Tokunaga ◽  
Shota Yasuda ◽  
Kenichi Fushimi ◽  
Munetaka Masuda
Keyword(s):  
Mitral Valve ◽  
Mitral Valve Surgery ◽  
Valve Surgery ◽  
Congenital Agenesis ◽  
The Right

Neurotrophic keratopathy associated with congenital agenesis of the corpus callosum

2012 ◽  
Vol 90 ◽  
pp. 0-0
Author(s):  
R HERRERO LATORRE ◽  
E GARCIA-MARTIN ◽  
G DE LA MATA ◽  
M SATUE ◽  
MP BAMBO ◽  
...  
Keyword(s):  
Corpus Callosum ◽  
Congenital Agenesis ◽  
Neurotrophic Keratopathy

scholarly journals Congenital Agenesis of the Left Lung: A Rare Case

2011 ◽  
Vol 1 ◽  
pp. 47 ◽  
Author(s):  
Tülin Durgun Yetim ◽  
Hanifi Bayaroğullari ◽  
Hülya Polat Yalçin ◽  
Vefik Arιca ◽  
Seçil Gunher Arιca
Keyword(s):  
Congenital Anomaly ◽  
Rare Case ◽  
Left Lung ◽  
Urogenital System ◽  
Pulmonary Agenesis ◽  
Rare Congenital Anomaly ◽  
Congenital Agenesis

Pulmonary agenesis is a rare congenital anomaly, the etiology of which is not clearly known. Other systemic comorbidities such as cardiovascular, gastrointestinal, musculoskeletal, and urogenital system anomalies can be observed in more than half of the patients. It is usually diagnosed during childhood. Diagnosis in adulthood is very rare. We present a case of pulmonary agenesis diagnosed in an adult.

scholarly journals An Unusual Occurrence of Multiple Dental Anomalies in a Single Nonsyndromic Patient: A Case Report

2012 ◽  
Vol 2012 ◽  
pp. 1-4 ◽  
Author(s):  
N. B. Nagaveni
Keyword(s):  
Chromosomal Abnormalities ◽  
Permanent Teeth ◽  
Simultaneous Occurrence ◽  
Third Molars ◽  
Dental Anomalies ◽  
Indian Girl ◽  
Multisystem Involvement ◽  
Unusual Occurrence ◽  
Mandibular Canine ◽  
Congenital Agenesis

Dental anomalies are the formative defects caused by genetic disturbances or environmental factors during tooth morphogenesis. Simultaneous occurrence of various multiple anomalies has been reported previously, particularly in cases of chromosomal abnormalities that often manifest with multisystem involvement. Very few cases of multiple anomalies have been documented in patients with no known generalized abnormalities. The present paper shows an unusual occurrence of a combination of dental anomalies like mandibular canine transmigration, taurodontism in permanent mandibular molars, congenital agenesis of 14 numbers of permanent teeth excluding third molars, canine impaction, primary molars with pyramidal roots, midline diastema and generalized microdontia in an apparently normal 13-year-old Indian girl.

The clinical significance of congenital Agenesis of the Corpus Callosum

1988 ◽  
Vol 3 (2) ◽  
pp. 189-200 ◽  
Author(s):  
E. D. Bigler ◽  
L. D. Rosenstein ◽  
M. Roman ◽  
N. L. Nussbaum
Keyword(s):  
Corpus Callosum ◽  
Clinical Significance ◽  
Congenital Agenesis

Venous status ulcers due to congenital agenesis of the inferior vena cava in a 16-year-old male

Vascular ◽  
2015 ◽  
Vol 24 (1) ◽  
pp. 106-108
Author(s):  
J Phair ◽  
E Trestman ◽  
J Stableford
Keyword(s):  
Magnetic Resonance ◽  
Inferior Vena Cava ◽  
Inferior Vena ◽  
Wound Care ◽  
Vena Cava ◽  
Compression Therapy ◽  
Venous Stasis ◽  
Presenting Symptoms ◽  
Duplex Imaging ◽  
Congenital Agenesis

We report a case of agenesis of the infrarenal inferior vena cava in a 16-year-old male presenting with venous stasis dermatitis and ulceration in the gaiter region bilaterally. Duplex imaging was performed revealing absence of infrarenal inferior vena cava and iliofemoral venous system. Magnetic resonance venography then confirmed the above findings along with revealing extensive lumbar and pelvic collateralization. This patient’s condition has been successfully managed conservatively with compression therapy and wound care. This case is a rare example of a congenital malformation of the inferior vena cava and represents the only reported case with presenting symptoms of venous stasis ulceration in a pediatric patient.

scholarly journals Complete agenesis of the right hemi-diaphragm in an adult: case report and literature review.

2021 ◽  
Vol 63 (3) ◽  
Author(s):  
Abdulsalam Yaseen Taha ◽  
Kalandar Kaznazani
Keyword(s):  
Mesh Repair ◽  
English Literature ◽  
Shortness Of Breath ◽  
Adult Case ◽  
Respiratory Compromise ◽  
Modest Improvement ◽  
Surgical Exploration ◽  
Serial Ct ◽  
Congenital Agenesis ◽  
The Right

Congenital agenesis of the hemi-diaphragm (AHD) in adults is rare and exceedingly so on the right side. Since its first recognition in 1959, no more than 9 cases have been published in the English literature by the year 2016. “Partial diaphragm agenesis” is actually large congenital diaphragmatic hernia (CDH) rather than true AHD. Respiratory compromise is the likely presentation, however, patients may survive for years without symptoms. Despite a straightforward clinical and radiographic diagnosis of AHD, the best method of repair is controversial. Herein, we present a case of complete right-sided AHD in a man of 54 diagnosed on surgical exploration 16 years earlier. Despite trans-thoracic mesh repair, the patient experienced just a modest improvement of his shortness of breath (SOB). Though the liver persisted high in the chest as shown by serial CT scans of the chest, polypropylene mesh was effective in preventing further visceral herniation. Adult patients with right-sided AHD always deserve operative intervention to avoid the potential complications.

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