المؤلفون: Rosa RF; Graduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, RS, Brazil.; Graduate Program in Biosciences, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, RS, Brazil.; Clinical Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA) and Complexo Hospitalar Santa Casa de Porto Alegre (CHSCPA), Porto Alegre, RS, Brazil., Correia EP; Graduation in Medicine, UFCSPA, Porto Alegre, RS, Brazil., Guimarães VB; Graduation in Medicine, UFCSPA, Porto Alegre, RS, Brazil., Trombetta JS; Graduation in Medicine, UFCSPA, Porto Alegre, RS, Brazil., Beltrão LA; Graduation in Medicine, UFCSPA, Porto Alegre, RS, Brazil., Lliguin KL; Graduation in Medicine, UFCSPA, Porto Alegre, RS, Brazil., de Mattos VF; Graduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, RS, Brazil., Rosa RC; Graduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, RS, Brazil., Zen PR; Graduate Program in Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, RS, Brazil.; Graduate Program in Biosciences, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, RS, Brazil.; Clinical Genetics, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA) and Complexo Hospitalar Santa Casa de Porto Alegre (CHSCPA), Porto Alegre, RS, Brazil.

المصدر: American journal of medical genetics. Part A [Am J Med Genet A] 2016 Jul; Vol. 170 (7), pp. 1945-6. Date of Electronic Publication: 2016 May 07.

نوع المنشور: Case Reports; Letter

بيانات الدورية: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE

مواضيع طبية MeSH: Gallbladder Diseases/*genetics , Trisomy 13 Syndrome/*genetics, Female ; Humans ; Infant ; Infant, Newborn ; Male

المؤلفون: Rosa RF; Clinical Genetics, Hospital Materno Infantil Presidente Vargas (HMIPV), Porto Alegre, Brazil; Department of Pathology, Universidade Federal de Ciências da Saúde de Porto Alegre (UFCSPA), Porto Alegre, Brazil; Clinical Genetics, UFCSPA and Complexo Hospitalar Santa Casa de Porto Alegre (CHSCPA), Porto Alegre, Brazil., Guimarães VB, Beltrão LA, Trombetta JS, Lliguin KL, de Mattos VF, Zen PR

المصدر: Pediatrics international : official journal of the Japan Pediatric Society [Pediatr Int] 2015 Apr; Vol. 57 (2), pp. e69-72. Date of Electronic Publication: 2015 Mar 25.

نوع المنشور: Case Reports; Journal Article; Review

بيانات الدورية: Publisher: Blackwell Science Asia Country of Publication: Australia NLM ID: 100886002 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1442-200X (Electronic) Linking ISSN: 13288067 NLM ISO Abbreviation: Pediatr Int Subsets: MEDLINE

مواضيع طبية MeSH: Mandibulofacial Dysostosis/*diagnosis , Pierre Robin Syndrome/*diagnosis, Fatal Outcome ; Humans ; Infant ; Infant, Newborn ; Male ; Mandibulofacial Dysostosis/complications ; Mandibulofacial Dysostosis/therapy ; Pierre Robin Syndrome/complications ; Pierre Robin Syndrome/therapy ; Respiration, Artificial ; Tracheostomy

SCR Disease Name: Acrofacial dysostosis, Nager type