Differential (Click to cross reference) atlanto-axial subluxation atrial enlargement basilar impression cerebral embolism cerebrovascular accident cerebrovascular accident, infancy and childhood children collagen vascular disease congenital heart disease cornea, abnormal cornea, opacity of cryptorchidism deafness developmental retardation dysmorphic ears, low set echocardiogram echocardiogram, transesophageal ejection fraction ejection fraction, abnormal familial gene mutation genetic neurologic disorders genetic screening genu valgum headache headache, recurrent hearing loss hemorrhage, intracranial, newborn hypertelorism intracranial hemorrhage kyphoscoliosis, neurologic causes of learning disability Morquio syndrome mucopolysaccharidoses myelopathy Noonan Syndrome osteogenesis imperfecta osteoporosis otosclerosis pectus carinatum pectus excavatum prognosis puberty, delayed root lesion, nerve sclerae, blue scoliosis sensorineural hearing loss short neck short stature spinal cord, compression of valvulopathy

Showing articles 0 to 6 of 6 Multivessel Cerebral Occlusion in Noonan Syndrome Stroke 56:e359-362, deLima, M.M.,et al, 2025 Mucopolysaccaridosis IV (Morquio Syndrome) , in The Metabolic Basis of Inherited Disease (Ed) 5th Ed. , McGraw-Hill, New York, p. 766, Stanbury,J.B., 1983 Osteogenesis Imperfecta, in Heritable Disorders of Connective Tissue (Ed) , 4th edition, The C. V. Mosby Company St. Louis, Chap. 8, pp. 390. , 1972, McKusick,V.A., 1972 Clinicopathologic Conference, Homocystinuria due to genetic mutations of the gene encoding cystathionine B-synthase (CBS) NEJM 378:941-948, Case 7-2018, 2018 Clinicopathologic Conference, Homocystinuria caused by Cystathionine B-Synthase Deficiency NEJM 375:1879-1890, Case 34-2016, 2016 A Clinical Study of Noonan Syndrome Arch Dis Child 67:178-183, Sharland, M.,et al, 1992 Showing articles 0 to 6 of 6