References
Gobbi G. Coeliac disease, epilepsy and cerebral calcifications. Brain Dev. 2005;27:189–200.
Simonati A, Battistella PA, Guariso G, Clementi M, Rizzuto N. Coeliac disease associated with peripheral neuropathy in a child: a case report. Neuropediatrics. 1998;29:155–158.
Papadatou B, Di Capua M, Gambarara M. Nervous system involvement in pediatric celiac patients. In: Mearin M, Mulder C, editorss. Celiac Disease. Dordrecht, The Netherlands: Kluwer Academic, 1991. P. 199–203.
Cakir D, Tosun A, Polat M, Celebisoy N, Gokben S, Aydogdu S, et al. Subclinical neurological abnormalities in children with celiac disease receiving a gluten-free diet. J Pediatr Gastroenterol Nutr. 2007;45:366–369.
Ruggieri M, Incorpora G, Polizzi A, Parano E, Spina M, Pavone P. Low prevalence of neurologic and psychiatric manifestations in children with gluten sensitivity. J Pediatr. 2008;152:244–249.
Korponay-Szabo IR, Halttunen T, Szalai Z, Laurila K, Kiraly R, Kovacs JB, et al. In vivo targeting of intestinal and extraintestinal transglutaminase 2 by coeliac autoantibodies. Gut. 2004;53:641–648.
Griffin M, Casadio R, Bergamini CM. Transglutaminases: nature’s biological glues. Biochem J. 2002;368:377–396.
Lerner A, Makhoul B, Eliakim R. Neurological manifestations of celiac disease in children, adults. Eur Neurol J. 2010;000:1–6.
Lytton S, Antiga E, Pfeiffer S, Matthias T, Poplawska AS, Ulaganathan K, et al. Neo-epitope tissue transglutaminase autoantibodies as a biomarker of the glutensensitive skin disease — Dermatitis herpetiformis. Clin Chim Acta. 2013;415:346–349.
Tursi A, Giorgetti GM, Iani C, Arciprete F, Brandimarte G, Capria A, et al. Peripheral neurological disturbances, autonomic dysfunction, and antineuronal antibodies in adult celiac disease before and after a gluten-free diet. Dig Dis Sci. 2006;51:1869–1874.
References
Sahin M. Tuberous Sclerosis. In: Kliegman RM, Stanton BF, St. Geme JW, Schor NF, Behrman RE, editors. Nelson Textbook of Pediatrics. 19th ed. Philadelphia: Saunders; 2012. p.2049–2051.
Irvine AD, Mellerio JE. Genetics and Genodermatoses: Tuberous sclerosis complex. In: Burns T, Breathnach, Cox N, Griffiths C, editors. Rook’s Textbook of Dermatology. 8th ed. UK: Willey-Blackwell; 2010. p.15. 21–25.
Spangler WJ, Cosgrove GR, Moumdjian RA, Montes JL. Cerebral arterial ectasia and tuberous sclerosis: case report. Neurosurgery. 1997;40:191–193.
Sabat SB, Cure J, Sullivan J, Gujrathi R. Tuberous sclerosis with multiple intracranial aneurysms: atypical tuberous sclerosis diagnosed in adult due to third nerve palsy. Acta Neurol Belg. 2010;110:89–92.
Guridi J, Tuñón M, Caballero C, Gallo-Ruiz A, Vázquez A, Zazpe I. Intracranial hemorrhage from an arteriovenous malformation (AVM) in a tuberous sclerosis patient. Neurologia. 2001;16:281–284.
Waga S, Yamamoto Y, Kojima T, Sakakura M. Massive hemorrhage in tumor of tuberous sclerosis. Surg Neurol. 1977;8:99–101.
Barbosa-Coutinho LM, Lima EL, Gadret RO, Ferreira NP. Massive intratumor hemorrhage in tuberous sclerosis. Autopsy study of a case. Arq Neuropsiquiatr. 1991;49:465–470.
Kalina P, Drehobl KE, Greenberg RW, Black KS, Hyman RA. Hemorrhagic subependymal giant cell astrocytoma. Pediatr Radiol. 1995;25:66–67.
Wadhwa R, Khan IS, Thomas JO, Nanda A, Guthikonda B. Hemorrhagic subependymal giant cell astrocytoma in a patient with tuberous sclerosis: case report and review of the literature. Neurol India. 2011;59:933–935.
Hoque R, Gonzalez-Toledo E, Minagar A, Kelley RE. Circuitous embolic hemorrhagic stroke: carotid pseudoaneurysm to fetal posterior cerebral artery conduit: a case report. J Med Case Rep. 2008;2:61.
References
Sengupta S, Das JK, Gangopadhyay A. Alagille syndrome with prominent skin manifestations. Indian J Dermatol Venereol Leprol. 2005;71:119–121.
Nigale V, Trasi SS, Khopkar US, Wadhwa SL, Nadkarni NJ. Alagille syndrome. A case report. Acta Derm Venereol. 1990;70:521–523.
Hadchouel M. Alagille syndrome. Indian J Pediatr. 2002;69:815–818.
Shendge H, Tullu MS, Shenoy A, Chaturvedi R, Kamat JR, Khare M, et al. Alagille syndrome. Indian J Pediatr. 2002;69:825–827.
Alagille D, Odievre M, Gautier M, Dommergues JP. Hepatic ductular hypoplasia associated with characteristic facies, vertebral malformations, retarded physical, mental, and sexual development, and cardiac murmur. J Pediatr. 1975;86:63–71.
Watson GH, Miller V. Arteriohepatic dysplasia: familial pulmonary arterial stenosis with neonatal liver disease. Arch Dis Child. 1973;48:459–466.
Oda T, Elkahloun AG, Pike BL, Okajima K, Krantz ID, Genin A, et al. Mutations in the human Jagged1 gene are responsible for Alagille syndrome. Nat Genet. 1997;16:235–242.
Kamath BM, Spinner NB, Piccoli DA. Alagille Syndrome. In: Suchy F, Sokol RJ, Balistreri WF, editors. Liver Disease in Children. Third ed. New York: Cambridge University Press; 2007. p. 326–345.
References
Jacqueline P, Scott RF, Jason H, John Z, Kristin L, Shery V. Neonatal pemphigus in an infant born to a mother with serologic evidence of both pemphigus vulgaris and gestational pemphigoid. J Am Acad Dermatol. 2009;60:1057–1062.
Michael H, Cassian S. Pathogenesis, Clinical Manifestations and Diagnosis of Pemphigus. Available from: URL: http//www.uptodate.com/store. Accessed July 7, 2013.
Sameera BKI, Yashodhara BM, Shashikiran U. Pemphigus vulgaris in a pregnant woman and her neonate. BMJ. 2012:2013:1–5.
Moncada B, Kettelsen S, Hernandez JL, Ramirez F. Neonatal pemphigus vulgaris: role of passively transferred pemphigus antibodies. Br J Dermatol. 1982;106:465–468.
Ian AG. Maternal Medicine: Medical Problems in Pregnancy, Dermatological disease in pregnancy, 1st ed. UK: Elsevier Health Sciences. 2007. P.276.
Author information
Authors and Affiliations
Corresponding authors
Rights and permissions
About this article
Cite this article
Boskovic, A., Stankovic, I., Purkait, R. et al. Case Reports. Indian Pediatr 51, 311–317 (2014). https://doi.org/10.1007/s13312-014-0385-0
Published:
Issue Date:
DOI: https://doi.org/10.1007/s13312-014-0385-0