Craniofrontonasal dysplasia syndrome: A rare case
Craniofrontonasal dysplasia syndrome (CFND) (Online Mendelian Inheritance in Man database Number 304110), first described as a distinct entity by Professor Michael Cohen from Canada in 1979, is a very rare X-linked inherited disorder characterized by abnormalities of the head and face (cranio-facial...
Main Authors: | Biswajit Biswas, Monojit Mondal, Atanu Roy, Rajib Das |
---|---|
Format: | Article |
Language: | English |
Published: |
Wolters Kluwer Medknow Publications
2015-01-01
|
Series: | Medical Journal of Dr. D.Y. Patil University |
Subjects: | |
Online Access: | http://www.mjdrdypu.org/article.asp?issn=0975-2870;year=2015;volume=8;issue=5;spage=672;epage=674;aulast=Biswas |
Similar Items
-
Chin wing osteotomy in a patient with craniofrontonasal dysplasia
by: L. Verstraete, et al.
Published: (2020-09-01) -
Trio-Based Whole-Exome Sequencing Identifies a De novo EFNB1 Mutation as a Genetic Cause in Female Infant With Brain Anomaly and Developmental Delay
by: Ji Yoon Han, et al.
Published: (2020-09-01) -
EPHRIN-B1 Mosaicism Drives Cell Segregation in Craniofrontonasal Syndrome hiPSC-Derived Neuroepithelial Cells
by: Terren K. Niethamer, et al.
Published: (2017-03-01) -
Camptomelic dysplasia: A case report
by: Koš Radmila, et al.
Published: (2007-01-01) -
Fibrocartilagenous dysplasia: A rare variant of fibrous dysplasia
by: Sajitha Kaliyath, et al.
Published: (2015-01-01)