Wolf-Hirschhorn syndrome

*Gene map locus 4p16.3

Chromosome 4p16.3 deletion syndrome

PRDS

Pitt syndrome

Pitt-Rogers-Danks syndrome

WHS

[Clinical features: severe mental and growth retardation; microcephaly; seizures; craniofacial anomalies; cardiac septal defects]

[Inheritance: isolated cases]

21 images [ from 1 to 15 ]	1 2 next


Mapping the Wolf-Hirschhorn Syndrome Phenotype Outside the Currently Accepted WHS Critical Region and Defining a New Critical Region, WHSCR-2	Wolf-Hirschhorn Syndrome	Wolf-Hirschhorn Syndrome
American Journal of Human Genetics	eMedicine	eMedicine


Comprehensive analysis of Wolf–Hirschhorn syndrome using array CGH indicates a high prevalence of translocations	Wolf-Hirschhorn syndrome facial dysmorphic features in a patient with a terminal 4p16.3 deletion telomeric to the WHSCR and WHSCR 2 regions	Widening the clinical spectrum of Pitt-Rogers-Danks/Wolf-Hirschhorn syndromes
European Journal of Human Genetics	European Journal of Human Genetics	Genetics and Molecular Biology


Oligomeganephronia in Wolf-Hirschhorn Syndrome	Wolf-Hirschhorn(4p-) syndrome	Wolf-Hirschhorn(4p-) syndrome
Indian Pediatrics	Indian Pediatrics	Indian Pediatrics


MSX1 Gene is Deleted in Wolf-Hirschhorn Syndrome Patients with Oligodontia	Deletion of a 760 kb region at 4p16 determines the prenatal and postnatal growth retardation characteristic of Wolf-Hirschhorn syndrome	Genotype–phenotype correlation in 21 patients with Wolf-Hirschhorn syndrome using high resolution array comparative genome hybridisation (CGH)
Journal of Dental Research	Journal of Medical Genetics	Journal of Medical Genetics


Mild Wolf-Hirschhorn syndrome: micro-array CGH analysis of atypical 4p16.3 deletions enables refinement of the genotype-phenotype map	Wolf-Hirschhorn syndrome	Wolf-Hirschhorn syndrome
Journal of Medical Genetics	Medical Genetics	Medical Genetics

21 images [ from 1 to 15 ]	1 2 next

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Edited by Aldo Campana, August 21, 2012