By Suresh Kotagal, Alma R. Bicknese, Marthand Eswara (auth.), Roger N. Rosenberg MD (eds.)
The newly revised, finished, four-color Atlas of medical Neurology is generally up-to-date on the subject of present literature. the hot 3rd version organizes the highest-quality photographs from the sphere of scientific neurology, together with medical syndromes, for neurologists and clinicians. The atlas highlights the big strides being made within the biologic realizing of neurologic affliction, masking developmental and genetic illnesses, neuroendocrine problems, severe care neurology, cerebrovascular illness, dementias, behavioral neurology, neuro-oncology, circulation issues, epilepsy, neuromuscular illnesses, infectious illnesses, neuroimmunology, neurotoxic problems, and headache. This quintessential assortment includes over 1300 photos together with algorithms, tables, charts, and schematic drawings.
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Extra info for Atlas of Clinical Neurology
Whether or not patients and families need to be counseled about avoiding tumbling, trampoline jumping, diving, high jump, and gymnastics varies from case to case and should be based upon the combined clinical and radiographic data  One must be careful to treat the patient, and not the radiograph! The bulk of patients with atlantoaxial instability are asymptomatic and need only periodic clinical follow-up . 30 Atlas of Clinical Neurology DYSOSTOSIS MULTIPLEX SECONDARY TO LYSOSOMAL STORAGE DISEASE Syndromes with Dysostosis Multiplex Disorder Deﬁcient Enzyme Elevated Urinary Mucopolysaccharide Inheritance Severity of Skeletal Changes Hurler (MPS I) B-Iduronidase Yes AR Severe Hunter (MPS II) Iduronate sulfatase Yes X-linked Severe Type A Heparan-N-sulfatase Yes/no AR Mild Type B B-N-acetylglucosaminidase Yes/no AR Mild Type C Acetyl CoA: B-glucosaminide acetyltransferase Yes/no AR Mild N-acetylglucosamine-6-sulfatase Yes/no AR Mild Type A Galactosamine-6-sulfatase Yes AR Severe, plus additional changes from other MPS Type B Sanﬁlippo (MPS III) Type D Morquio (MPS IV) C-Galactosidase Yes AR Severe Maroteaux-Lamy (MPS VI) Arylsulfatase B Yes AR Severe Sly (MPS VII) C-Glucuronidase Yes AR Severe I cell disease (ML II) N-acetylglucosamine phosphotransferase No AR Severe Pseudo-Hurler polydystrophy (ML III) N-acetylglucosamine phosphotransferase No AR Moderate B-Mannosidosis B-Mannosidase No AR Severe C-Mannosidosis C-Mannosidase No AR Mild/absent Sialidosis type II Sialidase No AR Severe Aspartylglucosaminuria Aspartylglucosaminidase No AR Mild Fucosidosis B-Fucosidase No AR Moderate Carbohydrate-deﬁcient glycoprotein syndrome type Ia Phosphomannomutase No AR Moderate to severe Figure 1-57.
14. Johnston MC: Understanding human embryonic development. In Human Malformations and Related Anomalies, vol 1. Edited by Stevenson RE, Hall JG, Goodman RM. New York: Oxford University Press; 1993:31–63. 15. Gellis SS, Feingold M, Tunnessen WW Jr, Raettig JA: Caudal regression d 1968, 116:407–408. syndrome: picture of the month. Am J Dis Child 16. Escobar LF, Weaver DD: Caudal regression syndrome. In Birth Defects Encyclopedia. Edited by Buyse L. Dover, MA: Center for Birth Defects Information Services in association with Blackwell Scientiﬁc Publications; 1990:296–297.
139. Ito M: A singular case of naevus depigmentosus systematicus bilateralis. Jpn J Dermatoll 1951, 61:131. 140. : Hypomelanosis of Ito: involvement of the chromosome aberrations in this syndrome. Ann Genett 1991, 34:30–32. 141. Taibjee SM, Bennett DC, Moss C: Abnormal pigmentation in hypomelanosis of Ito and pigmentary mosaicism: the role of pigmentary genes. Br J Dermatoll 2004, 151:269–282. 142. Wyburn-Mason R: Arteriovenous aneurysm of midbrain, retina, facial naevi and mental changes. Brain 1943, 66:163.