Add to ORKGINTRODUCTION: Sturge-Weber syndrome is a rather uncommon congenital condition that occurs spo-radically, characterized by the combination of ipsilateral angiomatous lesions of the face, oral soft tissues, and jaws with venous angioma of the leptomeninges over the cerebral cortex. However, the main clinical fea-tures of this syndrome are facial vascular cutaneous naevus, usually unilateral, which often follows the out-line distribution of the trigeminal nerve
Introduction: Sturge Weber Syndrome (SWS), known as encephalotrigeminal angiomatosis, is a rare neur...
Sturge-Weber syndrome (SWS), sometimes referred to as encephalotrigeminal angiomatosis, is a rare co...
Case report: We report the case of a child short in stature with brachydactyly and brachymorphy who ...
Introduction: The Syndrome of Sturge-Weber is a rare condition of congenital development, and is cha...
Abstract: Binder's Syndrome also known as Maxillo-Nasal Dysplasia is a developmental disorder ...
The characteristic findings seen in Sturge-Weber syndrome are thought to arise from an embryologic m...
Parry-Romberg syndrome (PRS) is a rare, acquired disorder characterized by progressive unilateral fa...
Introduction: The Syndrome of Sturge-Weber is a rare condition of congenital development, and is cha...
Apert syndrome is a rare autosomal dominant disorder characterized by craniosynostosis, craniofacial...
Sturge-Weber syndrome is a rare, sporadic disorder marked by an occipital leptomeningeal angioma tha...
Sturge-Weber syndrome (SWS) is a rare disorder that occurs sporadically with a frequency of 1:50,000...
VACTERL association is a useful acronym for a condition characterised by the sporadic, non-random as...
syndromes associated with overgrowth in childhood Review article Overgrowth syndromes comprise a div...
To the Editor Dr. Alomari gave us some valuable com-ments on the diagnosis of our patient recently r...
Introduction: Menkes disease is a rare X-linked recessive disorder of copper metabolism. It is chara...
Introduction: Sturge Weber Syndrome (SWS), known as encephalotrigeminal angiomatosis, is a rare neur...
Sturge-Weber syndrome (SWS), sometimes referred to as encephalotrigeminal angiomatosis, is a rare co...
Case report: We report the case of a child short in stature with brachydactyly and brachymorphy who ...
Introduction: The Syndrome of Sturge-Weber is a rare condition of congenital development, and is cha...
Abstract: Binder's Syndrome also known as Maxillo-Nasal Dysplasia is a developmental disorder ...
The characteristic findings seen in Sturge-Weber syndrome are thought to arise from an embryologic m...
Parry-Romberg syndrome (PRS) is a rare, acquired disorder characterized by progressive unilateral fa...
Introduction: The Syndrome of Sturge-Weber is a rare condition of congenital development, and is cha...
Apert syndrome is a rare autosomal dominant disorder characterized by craniosynostosis, craniofacial...
Sturge-Weber syndrome is a rare, sporadic disorder marked by an occipital leptomeningeal angioma tha...
Sturge-Weber syndrome (SWS) is a rare disorder that occurs sporadically with a frequency of 1:50,000...
VACTERL association is a useful acronym for a condition characterised by the sporadic, non-random as...
syndromes associated with overgrowth in childhood Review article Overgrowth syndromes comprise a div...
To the Editor Dr. Alomari gave us some valuable com-ments on the diagnosis of our patient recently r...
Introduction: Menkes disease is a rare X-linked recessive disorder of copper metabolism. It is chara...
Introduction: Sturge Weber Syndrome (SWS), known as encephalotrigeminal angiomatosis, is a rare neur...
Sturge-Weber syndrome (SWS), sometimes referred to as encephalotrigeminal angiomatosis, is a rare co...
Case report: We report the case of a child short in stature with brachydactyly and brachymorphy who ...