CLINICAL CASE Hidrocefalia Congénita: Síndrome de Gómez-López-Hernández, un síndrome subdiagnosticado. Caso clínico Camila

The Tuberous Sclerosis in the first descriptions by Désiré-Magloire Bourneville (1840-1909): Tuberous sclerosis and BournevilleFirst descriptions of tuberous

The neurocutaneous disorders are a group of clinically and genetically heterogeneous diseases that are characterized mainly by harmatomas and tumor growth, involving tissues

Journal ofNeurology, Neurosurgery, and Psychiatry, 1976, 39, 666-673 The tuberous sclerosis syndrome: clinical and EEG studies in 100 children G. PAMPIGLIONE AND E. J. MOYNAHAN

Tuberous sclerosis and Klippel-Trenaunay-Weber syndromes Association of two complete phakomatoses in a single individual B. TODD TROOST', PETER J. SAVINO, AND JOHN C.

430 The concept of tuberous sclerosis (TS) has evolved for over 160 years from clinical observations and anatomi- copathological studies to the introduction of molecular

Tuberous sclerosis presenting as a mass lesion in infancyJanet W. Bay, M.D. Department of Neurological Surgery A. David Rothner, M.D. Edward S. Sadar, M.D. Department of

Cutaneous Manifestations of Tuberous SclerosisSue Hake, DPM, FACFAS Department of Podiatry, Ochsner Medical Center–North Shore, Ochsner Clinic Foundation, Covington,

PII: 0007-117X(73)90029-2British Journal of Oral Surgey (1973), II, 126-130 TUBEROSE SCLEROSIS WITH UNILATERAL INVOLVEMENT OF THE MAXILLA AND MANDIBLE: A CASE REPORT DENNIS

Vol30_3.1.1IMAGE OF THE QUARTER CASE HISTORY An 11-year-old boy, whose father was known to have tuberous sclerosis (TS), presented with a first fit. On examination he had