TY  - JOUR
TI  - Wiedemann–Rautenstrauch Syndrome: Case Report
AB  - Neonatal-progeroid syndrome known as Wiedemann Rautenstrauch syndrome (WRS) is an extremely rare, autosomal recessive disorder. Neonatal progeroid disease characterized by progeroid appearance growth retardation, lipodystrophy, an unusual face (triangular shape, sparse hair, small mouth, macrocephaly, pointed jaw), thin skin, hard and thick joints and dental anomalies (newborn tooth; hypodontics). A 5-year-old boy case diagnosed with hypodontics is presented. In this case, a child prosthesis was performed to facilitate the nutrition of the patient and to increase the quality of life.
AU  - Derdiyok, Cansu
AU  - Ipek, Irem
AU  - OZNURHAN, Fatih
DO  - 10.7126/cumudj.1127344
PY  - 2022
JO  - Cumhuriyet Dental Journal 
VL  - 25
IS  - 3
SN  - 1302-5805
SP  - 282
EP  - 284
DB  - TRDizin
UR  - http://search/yayin/detay/1129543
ER  -