Results 61 to 70 of about 39,335 (209)

Klippel-Trénaunay Syndrome with Intracranial Arteriovenous Malformation: A Rare Presentation

open access: yesCase Reports in Radiology, 2014
Klippel-Trénaunay syndrome (KTS) is a rare vascular congenital anomaly affecting less than 200,000 people in the United States. Vascular malformations associated with KTS tend to affect slow flow systems: venous, capillary, and lymphatic systems.
Mahniya F. Sadiq   +4 more
doaj   +1 more source

Congenital short bowel syndrome: Clinical aspects by systematic review

open access: yesJPGN Reports, EarlyView.
Abstract Objectives Congenital short bowel syndrome (CSBS) is a rare intestinal disorder characterized by inborn shortening of the bowel with mainly mutations in Coxsackie and Adenovirus receptor‐like membrane protein (CLMP) and Filamin A (FLNA) genes.
Barblin Remund   +2 more
wiley   +1 more source

Death Related to a Congenital Vascular Anomaly of Pulmonary Hamartoma Type: Malpractice or Tragic Fatality? [PDF]

open access: yesMedicina (Kaunas), 2021
Marrone M   +5 more
europepmc   +1 more source

Genetic sequencing of children with malrotation and midgut volvulus: A cross‐sectional study

open access: yesJPGN Reports, EarlyView.
Abstract Objectives Intestinal malrotation with midgut volvulus can cause a particularly severe form of pediatric intestinal failure and is often a cause of ultra‐short bowel syndrome (SBS), with longer dependence on parenteral nutrition. While malrotation can be found in several genetic syndromes, most occurrences of this condition are not associated ...
Jonathan A. Salazar   +9 more
wiley   +1 more source

Ingrown Toenails in Infants and Children: Developmental Variants and Age‐Specific Management

open access: yesJEADV Clinical Practice, EarlyView.
ABSTRACT Infantile ingrown toenails are a common pediatric nail disorder encompassing a spectrum of developmental, anatomical, and mechanical conditions, including congenital malalignment of the great toenail (CMGT), hypertrophy of the lateral nail folds, distal nail embedding, and early inflammatory forms of onychocryptosis.
Lourdes Navarro, Minia Campos
wiley   +1 more source

Isolated Pulmonary Artery Sling Diagnosed in Adulthood

open access: yesClinical Case Reports
Although pulmonary artery sling (PAS) is typically a congenital vascular ring anomaly detected in early childhood, its isolated form can also be diagnosed in adulthood.
Emine Afsin   +2 more
doaj   +1 more source

Arteriovenous fistula between descending aorta and left inferior pulmonary vein: Closure with vascular plugs

open access: yesTürk Kardiyoloji Derneği Arşivi, 2016
Echocardiography revealed systemic artery to pulmonary venous fistula, a rare vascular anomaly, in a 20-month-old girl, and multislice computed tomography angiography (CTA) was performed to rule out congenital heart disease.
Mustafa Kösecik   +2 more
doaj   +1 more source

Robot-assisted nephroureterectomy in a patient with left-sided inferior vena cava: a case report

open access: yesUrology Case Reports
Left-sided inferior vena cava (LS-IVC) is a rare congenital vascular anomaly that can complicate retroperitoneal surgery because of altered venous and lymphatic anatomy. We report a case of robot-assisted nephroureterectomy performed in a patient with LS-
Masahiro Katsui   +3 more
doaj   +1 more source

Orbital Lymphatic Malformations Are Associated With Intracranial Vascular Anomalies

open access: yesThe Laryngoscope, EarlyView.
In this retrospective series, all seven patients with orbital lymphatic malformations had intracranial vascular anomalies consistent with cerebrofacial venous metameric syndrome and hotspot PIK3CA variants identified through tissue‐based sequencing. Five patients treated with alpelisib experienced symptom improvement within 6 months.
Kelsey A. Loy   +11 more
wiley   +1 more source

Intraoperative Hemodynamic Instability in a Patient With Ebstein’s Anomaly Complicated With Eisenmenger Syndrome

open access: yesCase Reports in Cardiology
Ebstein’s anomaly is a rare congenital displacement of the tricuspid valve resulting in atrialization of the right ventricle. About half of the patients with Ebstein’s anomaly also have atrial septal defects, which may lead to chronic shunting and ...
Leonardo A. Marquez Roa   +4 more
doaj   +1 more source

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