2011, Number 3
<< Back Next >>
Rev Odont Mex 2011; 15 (3)
Adams-Oliver syndrome. Case report
Godínez BM, Parés VG, Hinojosa AA, Yamamoto NA
Language: Spanish
References: 47
Page: 175-182
PDF size: 415.99 Kb.
ABSTRACT
Adams Oliver syndrome (AOS) is a rare disease characterized by congenital scalp defects, terminal transverse limb malformations, and cutis marmorata telangiectatica, whose treatment requires a multidisciplinary focus to improve the patient s quality of life. We report the case of a child afflicted with varied manifestations of AOS including craniofacial alterations in the form of facial fissure, bilateral cleft lip and grade III cleft palate. Therapeutic focus of this case was approached in the dental area, taking into account the patient s systemic conditions. The process was divided into five phases taking into consideration the patient s current age, as well as intraoral and craniofacial circumstances.
REFERENCES
Hona J, Frieden MD. Clinical review. Aplasia cutis congenital: A clinical review and proposal for classification. J Am Acad Dermatol 1987; 4 (4): 646-60.
Calduch LJR. Aplasia cutis congenital de cuero cabelludo. Estudio clínico de 35 pacientes y su relación con los defectos de la línea media. (Tesis doctoral). Universitat de Valencia. Facultad de Medicina 2005.
Cordon M. Extrait d’ une lettre au sujet de trois enfants de la meme mere nés avee partie des extremites denuee de peau. J Med Chir Pharmacie 1767; 26: 556-557.
Pérez LC, Urbina FG, Roa JA. Aplasia cutis congénita: a propósito de cuatro casos. Rev Chil Pediatr 2001: 72 (4).
Jaeggi E, Kind C, Morger R. Congenital scalp and skull defects with terminal transverse limb anomalies (Adams-Oliver syndrome): report of tree additional cases. Eur J Pediatr 1990; 149 (8): 565-6.
National Center for Biotechnology Information. Adams-Oliver syndrome. http://www.ncbi.nlm.nig.gov
Online Mendel Ian Inheritance in Man. Adams-Oliver Síndrome; AOS. http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=100300.
Luján JI, Ibarra AG, Méndez FV. Síndrome de Adams-Oliver. Reporte de un caso. Rev Hosp Jua Mex 2004; 71 (3): 124-7.
Mempel M, Abeck D, Lange I, Strom K. The wide spectrum of clinical expression in Adams-Oliver syndrome: a report of two cases. British Journal of Dermatology 1999; 140: 1157-1160.
Adams FH, Oliver CP. Hereditary deformities in man due to arrested development. J Hered 1945; 36: 3-7.
Scrubabu NMD. The syndrome of aplasia cutis congenital with terminal, transverse defect of limbs. Brief clinical and laboratory observations. The journal of Pediatrics 1975; 87 (1): 79-82.
Martínez-Frías ML, Arroyo-Carrera I, Muñoz-Delgado NJ. The Adams-Oliver syndrome in Spain: the epidemiological aspects. An Esp Pediatr 1996; 45 (1): 57-61.
Whitley CB, Gorlin RJ. Adams-Oliver syndrome revisited. Am J Med Genet 1991; 40 (3): 319-26.
Barcela SL. Síndrome de Adams-Oliver. Caso Clínico. Revista Salud Pública y Nutrición. Edición Especial. XXIX Congreso Nacional de Genética Humana 2004. URL: http://www.respyn.uanl.mx/especiales/2005/ee-05-2005/carteles/genetica_clinic_a1.htm.
Bilginer B, Onal MB, Bahadir S, Akalan N. Aplasia cutis congenital of the scalp, skull and dura associated with Adams-Oliver syndrome. Turkish Neurosurgery 2008; 18 (2): 191-193.
Salvador J, Casas J. Catálogo de síndromes polimalformativos congénitos con anomalías oculares. Instituto Municipal de Salud Pública. Ayuntamiento de Barcelona. http://www.aspb.es/quefem/docs/Catal_sind_polimalformativos.
Temtamy SA, Aglan MS, Ashour AM, Zaki MS. Adams-Oliver syndrome: further evidence of an autosomal recessive variant. Clin Dysmorphol 2007; 16 (3): 141-9.
Ortavik KH, Strömme P, Spetalen S, Flage T, Westvik J, Vesterhus P, Skjeldad O. Aplasia cutis congenita associated with limb, eye, and brain anomalies in sibs: a variant of the Adams-Oliver syndrome? Am J Med Genet 1995; 59 (1): 92-5.
Prothero J, Nicholl R, Wilson J, Wakeling EL. Aplasia cutis congenital, terminal limb defects and falciform retinal folds: confirmation of a distinct syndrome of vascular disruption. Clin Dysmorphol 2007; 16 (1): 39-41.
Fayol L, Garcia P, Denis D, Philip N, Simeoni U. Adams-Oliver syndrome associated with cutis marmorata telangiectatica congenital and congenital cataract: a case report. Am J Perinatol 2006; 23 (39): 197-200.
McGoey RR, Lacassie Y. Adams-Oliver syndrome in siblings with central nervous system fingings, epilepsy, and developmental delay: refining the features of a severe autosomal recessive variant. Am J Med Genet A 2008; 146 (4): 488-91.
Girard M, Amiel J, Fabre M, Pariente D, Lyonnet S, Jacquemin E. Adams-Oliver syndrome and hepatoportal sclerosis: occasional association or common mechanism? Am J Med Genet A 2005; 135 (2): 186-9.
Sun-Young Jun, Shin Kwang Khang. An autopsy case of Adams-Oliver syndrome. J Korean Med Set 2000; 15: 482-4.
Rajabian MH, Aghaei SMD. Adams-Oliver syndrome and isolated aplasia cutis congenital in two sibs. Dermatology Online Journal 2001: 12 (6).
Roca OJL, Cendán MI, Alonso LF, Ferrero OME, Lantigua CA. Caracterización clínica del labio hendido con fisura palatina o sin ésta en Cuba. Rev Cubana Pediatr 1998: 70 (1).
Gomes LB, Castro J, Matos M, Numes A, Furtado J, Barrueco MC. Lesion of the central nervous system in Adams-Oliver’s syndrome. Acta Med Port 2001; 14 (1): 89-94. Acta Med Port 2001; 14 (4): 455-6.
Bamforth JS, Kaurah P, Byrne J, Ferreir P. Adams Oliver syndrome: a family with extreme variability in clinical expression. Am J Med Genet 1994; 49 (4): 393-6.
Piazza AJ, Blackston D, Sola A. A case of Adams-Oliver syndrome with associated and pulmonary involvement: further evidence of vascular pathology? Am J Med Genet A 2004; 130A (2): 172-5.
Zapata HH, Sletten LJ, Pierpont ME. Congenital cardiac malformations in Adams-Oliver syndrome. Clin Genet 1995; 47 (2): 80-4.
Papadopoulou E, Sifakis S, Raissaki M, Germanakis I, Kalmanti M. Antenatal and postnatal evidence of periventricular leukomalacia as a further indication of vascular disruption in Adams-Oliver syndrome. Am J Med Genet A 2008; 146A (19): 2545-2550.
Lin AE, Westgate MN, van der Velde ME, Lacro RV, Holmes LB. Adams-Oliver syndrome associated with cardiovascular malformations. Clin Dysmorphol 1998; 7 (4): 235-41.
Farrell SA, Warda LJ, LaFlair P, Szymonowicz W. Adams-Oliver syndrome: a case with juvenile chronic myelogenous leukemia and chylothorax. Am J Med Genet 1993; 47 (8): 1175-9.
Verdyck P, Blaumeiser B, Holder-Espinasse M. Adams-Oliver syndrome: clinical description of a four-generation family and exclusion of five candidate genes. Clin Genet 2006; 69: 86-92.
Narang T, Kanwr AJ, Dogra S. Adams-Oliver syndrome: a sporadic occurrence with minimal disease expression. Pediatr Dermatol 2008; 25 (1): 115-6.
Becker R, Kunze J, Horn D, Gasiorek-Wiens. Autosomal recessive type of Adams-Oliver syndrome: prenatal diagnosis. Ultrasound Obstet Gynecol 2002; 20: 506-510.
Verdyck P, Holder-Espinasse M, Van Hull W, Wuyts W. Clinical and molecular analysis of nine families with Adams-Oliver syndrome. European Journal of Human Genetics 2003; 11: 457-463.
Toriello HV, Graff RG, Florentine MF. Scalp and limb defects with cutis marmorata telangiectatica congenital: Adams-Oliver syndrome? Am J Med Genet 1988; 29: 269-76.
Jaeggi E, Kind C, Morger R. Congenital scalp and skull with terminal transverse limb anomalies (Adams-Oliver syndrome): report of tree additional cases. Eur J Pediatr 1990; 149 (8): 565-6.
Keymolen K, De Smet L, Bracke P, Fryns JP. The concurrence of ring constrictions in Adams-Oliver syndrome: additional evidence for vascular disruption as common pathogenetic mechanism. Genet Couns 1999; 10 (3): 295-300.
Fryns JP, Legius E, Demaerel P, Van den Berghe H. Congenital scalp defect, distal limb reduction anomalies, right spastic hemiplegia and hipoplasia of the left arteria cerebro media. Further evidence that interruption of early embryonic blood supply may result in Adams-Oliver (plus) syndrome. Clin Genet 1996; 50 (6): 505-9.
Swartz EN, Sanatani S, Sandor GG, Schreiber RA. Vascular abnormalities in Adams-Oliver syndrome: a cause or effect? Am J Med Genet 1999; 82 (1): 49-52.
Der Kaloustian VM, Hoyme HE, Hogg H, Entin MA, Guttmacher AE. Possible common pathogenetic mechanisms for Poland sequence and Adams-Oliver syndrome. Am J Med Genet 1991; 38 (1): 69-73.
Suárez O, López-Gutiérrez JC, Andrés A, Barrera S, Encinas JL, Luis A, Soto-Bauregard C, Días M, Ros Z. Aplasia cutis congenital: surgical treatment and results in 36 cases. Cir Pediatr 2007; 20 (3): 151-5.
Rick A, Nishimura, Blase A, Carabello, David P, Faxon, Michael D, Freed, Bruce W Lytle, Patrick T. O’Gara, Robert A, O’Rourke. Guideline update on valvular heart disease: Focused Update on Infective Endocarditis. JACC 2008; 52 (8): 676-85.
Savarirayan R, Thompson EM, Abbott KJ, Moore MH. Cerebral cortical dysplasia and digital constriction rings in Adams-Oliver syndrome. Am J Med Genet 1999; 86 (1): 15-9.
Davis PM, Buss PW, Simpson BA, Sykes. Near fatal hemorrhage from the superior sagital sinus in Adams-Oliver syndrome. Archives of Disease in Childhood 1993; 68: 433.