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See Latest ArticlesTSC2/PKD1 Contiguous Gene Syndrome: A Report of 2 Cases With Emphasis on Dermatopathologic Findings
American Journal of Dermatopathology, 07/27/09
Pizinger K et al. – The authors report 2 sporadic cases form of TSC2/PKD1 contiguous gene syndrome, with emphasis on dermatopathologic findings. Clinical awareness and appropriate molecular investigation of TSC2/PKD1 contiguous gene syndrome is necessary in all patients with a typical phenotype of TSC in infancy, adolescence, or adult age, because of severity of the renal alterations.
Today in Basic Science/Genetics...keeping you current
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Neonatal seizures and Long QT Syndrome: A cardiocerebral channelopathy
Epilepsia, 11/10/09
Genetic forms of hypopituitarism and their manifestation in the neonatal period
Early Human Development, 10/30/09
BTNL2 gene polymorphisms may be associated with susceptibility to Kawasaki disease and formation of coronary artery lesions in Taiwanese children
European Journal of Pediatrics, 11/05/09
Today in Pediatric Dermatology...keeping you current
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Skin fusion on the fingers and toes of an adolescent girl
The Clinical Advisor, 09/10/09
Irregular purplish blue markings on the limbs of a newborn
The Clinical Advisor, 11/11/09
Severe pruritic rash, fever, and malaise
The Clinical Advisor, 11/10/09
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