Rubrica iconografica
Un neonato “extralarge” (sindrome di Sotos)
E. Scaffidi
Marzo 2003 - pagg. 189 -190
Classificazione MeSH
Bibliografia
1. Smith DW. Recognizable patterns of human
malformation. 3rd edition: WB Saunder
Co,1982.
2. Robertson SP, Bankier A. Sotos syndrome and cutis laxa. J Med Genet 1999 Jan;36(1): 51-6.
3. Inoue K, Kato S, Numaga J, et al. Optic disk pallor and retinal atrophy in Sotos syndrome (cerebral gigantism). Am J Ophthalmol 2000 Dec;130(6):853-4.
4. Yen MT, et al. Unilateral glaucoma in Sotos syndrome (cerebral gigantism). Am J Ophthalmol 2000 Dec;130(6):851-3.
5. Leonard NJ, et al. Sacrococcygeal teratoma in two cases of Sotos syndrome. Am J Med Genet 2000 Nov.13;95(2):182-4.
6. Marci M, Ziino O, D’Angelo, et al. Fibroma of the left ventricle in a patient with Sotos syndrome. Echocardiography 2001 feb; 18(2): 171-3.
7. Neri G, Steindl K, Cappa M. Cause genetiche di iperaccrescimento fetale. Atti del VII Congresso Nazionale S.I.N. Chieti, Giugno 2001;25:26.
8. Lin Ae, Liu Q, Mannheim GB, et al. Exclusion of growth factor gene mutations as a common cause of Sotos syndrome. Am J Med Genet 2001 Jan 1;98(1):101-2.
2. Robertson SP, Bankier A. Sotos syndrome and cutis laxa. J Med Genet 1999 Jan;36(1): 51-6.
3. Inoue K, Kato S, Numaga J, et al. Optic disk pallor and retinal atrophy in Sotos syndrome (cerebral gigantism). Am J Ophthalmol 2000 Dec;130(6):853-4.
4. Yen MT, et al. Unilateral glaucoma in Sotos syndrome (cerebral gigantism). Am J Ophthalmol 2000 Dec;130(6):851-3.
5. Leonard NJ, et al. Sacrococcygeal teratoma in two cases of Sotos syndrome. Am J Med Genet 2000 Nov.13;95(2):182-4.
6. Marci M, Ziino O, D’Angelo, et al. Fibroma of the left ventricle in a patient with Sotos syndrome. Echocardiography 2001 feb; 18(2): 171-3.
7. Neri G, Steindl K, Cappa M. Cause genetiche di iperaccrescimento fetale. Atti del VII Congresso Nazionale S.I.N. Chieti, Giugno 2001;25:26.
8. Lin Ae, Liu Q, Mannheim GB, et al. Exclusion of growth factor gene mutations as a common cause of Sotos syndrome. Am J Med Genet 2001 Jan 1;98(1):101-2.