Objectives. To describe imaging findings of central nervous system involvement in patients with lipoid proteinosis. Methods. Patients with lipoid proteinosis followed in the dermatology and neurology departments of the State University of Campinas between 2002 and 2004 were evaluated using high-resolution MRI and computerized tomography (CT). Results. We reviewed the charts of three patients (two women) with lipoid proteinosis with, ages ranging from 5 to 44 years. Symptomatic disease duration ranged from 2 to 39 years. MRI scans showed hypointense signal in FLAIR and T2 images in the amygdalae in two of three patients. Brain CT scans from two patients showed that MRI findings were calcifications. The calcification was more evident in patie...
SummaryWe report the clinical, neuroradiological, and molecular genetic findings in a patient with l...
Lipoid proteinosis is a rare chronic inherited, autosomal, recessive metabolic disorder characterize...
We report the clinical, neuroradiological, and molecular genetic findings in a patient with lipoid p...
AbstractLipoid proteinosis is a rare, autosomal-recessive, genetic disorder characterized by multisy...
Lipoid proteinosis is a rare autosomal recessive genodermatosis characterized by the deposition of h...
Lipoid proteinosis (LP) is a very rare autosomal-recessive disease characterized by multisystem invo...
Lipoid proteinosis is a rare autosomal recessive disorder caused by mutations in ECM1, encoding extr...
AbstractLipoid proteinosis is an autosomal recessive disease of abnormal deposition of glycoprotein ...
Lipoid proteinosis was diagnosed in two daughters of a consanguinous marriage on the basis of geneti...
SUMMARY Lipoid proteinosis (Urbach-Wiethe disease) is a rare autosomal recessive disorder associated...
Abstract Urbach–Wiethe (or lipoid proteinosis) disease (UWD) is a rare autosomal recessive disorder ...
Lipoid proteinosis (LP) is a rare autosomal recessive genodermatosis. Genetic mutation leads to depo...
An 18-year-old male patient of consanguineous parents, delivered at full-term by cesarean section an...
Lipoid proteinosis (LP) is a rare, inherited condition that progresses gradually with multisystemic ...
Typical findings in this rare genodermatosis Lipoid proteinosis (LiP) results from a multisystem int...
SummaryWe report the clinical, neuroradiological, and molecular genetic findings in a patient with l...
Lipoid proteinosis is a rare chronic inherited, autosomal, recessive metabolic disorder characterize...
We report the clinical, neuroradiological, and molecular genetic findings in a patient with lipoid p...
AbstractLipoid proteinosis is a rare, autosomal-recessive, genetic disorder characterized by multisy...
Lipoid proteinosis is a rare autosomal recessive genodermatosis characterized by the deposition of h...
Lipoid proteinosis (LP) is a very rare autosomal-recessive disease characterized by multisystem invo...
Lipoid proteinosis is a rare autosomal recessive disorder caused by mutations in ECM1, encoding extr...
AbstractLipoid proteinosis is an autosomal recessive disease of abnormal deposition of glycoprotein ...
Lipoid proteinosis was diagnosed in two daughters of a consanguinous marriage on the basis of geneti...
SUMMARY Lipoid proteinosis (Urbach-Wiethe disease) is a rare autosomal recessive disorder associated...
Abstract Urbach–Wiethe (or lipoid proteinosis) disease (UWD) is a rare autosomal recessive disorder ...
Lipoid proteinosis (LP) is a rare autosomal recessive genodermatosis. Genetic mutation leads to depo...
An 18-year-old male patient of consanguineous parents, delivered at full-term by cesarean section an...
Lipoid proteinosis (LP) is a rare, inherited condition that progresses gradually with multisystemic ...
Typical findings in this rare genodermatosis Lipoid proteinosis (LiP) results from a multisystem int...
SummaryWe report the clinical, neuroradiological, and molecular genetic findings in a patient with l...
Lipoid proteinosis is a rare chronic inherited, autosomal, recessive metabolic disorder characterize...
We report the clinical, neuroradiological, and molecular genetic findings in a patient with lipoid p...