Beckwith-Wiedemann Syndrome

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Recent Publications on Beckwith-Wiedemann Syndrome:
Nasal encephalocele in a child with Beckwith-Wiedemann syndrome. Beckwith-Wiedemann syndrome (BWS) is a rare congenital syndrome...	11th July, 2008	Rudolf Magnus Institute of Neuroscience, University Medical Center	J Neurosurg Pediatrics. 2008 Jun;1(6):485-7. DOI Direct Link
Prenatal diagnosis of fetal hepatoblastoma: case report and review of the literature. Hepatoblastoma is the most common liver malignancy in childhood. The...	26th June, 2008	Department of Maternal-Fetal Medicine, Sharp Mary Birch Hospital for	J Ultrasound Med. 2008 Jul;27(7):1095-8.
Prenatal sonographic findings of congenital adrenal cortical adenoma. The differential diagnosis of prenatally diagnosed adrenal masses includes...	26th June, 2008	Divisions of Maternal-Fetal Medicine, State University of New York,	J Ultrasound Med. 2008 Jul;27(7):1091-3.
[Anesthetic management of a pediatric patient with Beckwith-Wiedemann syndrome accompanied by macroglossia] We report the anesthetic management of an infant with Beckwith-Wiedemann...	25th June, 2008	Department of Anesthesiology, Hyogo Prefectural Child Hospital, Kobe	Masui. 2008 Apr;57(4):464-6.
Epigenotype, phenotype, and tumors in patients with isolated hemihyperplasia. OBJECTIVE: To investigate whether epigenotyping of patients with isolated...	24th June, 2008	Department of Clinical Genetics, Academic Medical Centre, Amsterdam, The	J Pediatr. 2008 Jul;153(1):95-100. Epub 2008 Mar 7. DOI Direct Link
→View more research publications.

Beckwith-Wiedemann Syndrome Clinical Trials:
Genetics of Wilms' Tumor and/or the Associated Conditions of Aniridia, Hemihypertrophy, and Genitourinary Anomalies	Wilms' Tumor;   Aniridia
Hepatoblastoma Biology Study and Tissue Bank	Hepatoblastoma Intervention: Procedure: Biology Study and Tissue Banking

Beckwith-Wiedemann Syndrome Patents:
US Patent No.	Title
6124104	Chromosome 13-linked breast cancer susceptibility gene
6316599	Localization and characterization of the Wilms' tumor gene
6342357	Alterations in the long QT syndrome genes KVLQT1 and SCN5A and methods for detecting same
6369295	Uses of transgenic mouse containing a type X collagen mutant
6420124	KVLQT1--a long qt syndrome gene
→View more patents.

BioPortfolio Ltd. offers e-mail and postal lists for Beckwith-Wiedemann Syndrome scientists - we have details of around 90 individuals working on Beckwith-Wiedemann Syndrome .

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