Depression and hyperactivity in two patients with craniofrontonasal syndrome

Am J Med Genet A. 2016 Mar;170(3):799-800. doi: 10.1002/ajmg.a.37482. Epub 2015 Nov 19.

Authors

Matthias Fischer¹, Patricia-Stefanie Bänsch², Stefan Unterecker¹, Marcel Romanos², Jürgen Deckert¹

Affiliations

¹ Department of Psychiatry, Psychosomatics and Psychotherapy, University of Wuerzburg, Germany.
² Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University of Wuerzburg, Germany.

PMID: 26586496
DOI: 10.1002/ajmg.a.37482

No abstract available

Publication types

Case Reports

MeSH terms

Adult
Child, Preschool
Craniofacial Abnormalities / diagnosis
Craniofacial Abnormalities / genetics
Craniofacial Abnormalities / physiopathology*
Craniofacial Abnormalities / psychology*
Depression / diagnosis
Depression / genetics
Depression / psychology*
Ephrin-B1 / genetics
Female
Humans
Hyperkinesis / diagnosis
Hyperkinesis / genetics
Hyperkinesis / physiopathology*
Mutation
Phenotype

Substances

EFNB1 protein, human
Ephrin-B1

Supplementary concepts

Craniofrontonasal dysplasia