Eur Rev Med Pharmacol Sci 2020; 24 (23): 11998-12000
DOI: 10.26355/eurrev_202012_23987

Low-birth-weight infant with Antley-Bixler syndrome-like phenotype caused by POR mutation: a rare case report

G. Imataka, M. Fujisawa, R. Kuribayashi, G. Ichikawa, Y. Watabe, H. Suzumura, O. Arisaka, S. Yoshihara

Department of Pediatrics, Dokkyo Medical University, Tochigi, Japan. geo@dokkyomed.ac.jp

Free PDF Download

To cite this article

G. Imataka, M. Fujisawa, R. Kuribayashi, G. Ichikawa, Y. Watabe, H. Suzumura, O. Arisaka, S. Yoshihara
Low-birth-weight infant with Antley-Bixler syndrome-like phenotype caused by POR mutation: a rare case report

Eur Rev Med Pharmacol Sci
Year: 2020
Vol. 24 - N. 23
Pages: 11998-12000
DOI: 10.26355/eurrev_202012_23987

Keywords Related articles:

  1. Goldenhar syndrome: a new case expanding the phenotype by costal agenesis and pulmonary hypoplasia
  2. Usefulness of DuoPAP in the treatment of very low birth weight preterm infants with neonatal respiratory distress syndrome
  3. Del(18)(q12.2q21.1) syndrome: a case report and clinical review of the literature
  4. Fibrinogenopenia caused by Tigecycline: a case report
  5. Diagnosis and treatment of a rare case of adenomatoid odontogenic tumor in a young patient affected by attenuated familial adenomatosis polyposis (aFAP): case report and 5 year follow-up