Author: Roach, E. S. (Ewell Steve) & Miller, Van S.; editors:
Title: Neurocutaneous Disorders
Description: Cambridge, Cambridge University Press, (2004). orig.boards. 29x21cm, xvii,338 pp. Textual illustrations.. Some light rubbing to cover corner. VG. ¶ Contents: Genetics of neurocutaneous disorders; Syndrome/clinical recognition; Neurofibromatosis type 1; Neurofibromatosis type 2 D.; Tuberous sclerosis complex; Von Hippel-Lindau disease; Neurocutaneous melanosis; Basal Cell Nevus syndrome; Epidermal Nevus syndrome; Multiple endocrine neoplasia type 2; Ataxia-telangiectasia; Incontinentia pigmenti; Hypomelanosis of Ito; Cowden disease; Pseudoxanthoma elasticum; Ehlers- Danlos syndrome; Progeria; Blue Rubber Bleb Nevus syndrome; Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu); Hereditary neurocutanous angiomatosis; Cutaneous hemangiomas: vascular anomaly complex; Sturge- Weber syndrome ; Lesch-Nyhan syndrome; Multiple carboxylase deficiency; Homocystinuria due to cystathionine-synthase (CBS) deficiency; Fucosidosis;Menkes Kinky Hair syndrome/Menkes disease; Xeroderma pigmentosum, Cockayne syndrome and trichothiodystrophy; Cerebrotendinous xanthomatosis; Adrenoleukodystrophy; Peroximal disorders; Familial dysautonomia; Fabry disease; Giant axonal neuropathy; Chediak-Higashi syndrome; Encephalocraniocutaneous lipomatosis; Cerebello-Trigemino-Dermal dysplasia;Coffin-Siris syndrome; Lipoid proteinosis; Macrodactyl-nerve fibrolipoma.

Keywords: Neurocutaneous Syndromes, Dermatology, Skin Diseases, Disorders, Genetics, Diagnosis, Therapy, Medicine,