Infantile Huntington’s Disease

Summary

Although rare, Huntington’s disease must be considered along with the established degenerative disorders of white and gray matter peculiar to the pediatric population when one examines an infant or child with progressive motor deterioration, rigidity, mental retardation and behavioural abnormalities.

Keywords

Huntington's disease, Disease, Pediatrics, Medicine, Presentation (obstetrics)

References

[Huntington's chorea in children].T. Schönfelder — 1966
Huntington's choreaJames A. Mills, Adam L. Orr, J. R. Whtttier — 1969
HUNTINGTON'S CHOREA IN CHILDHOOD.George A. Jervis — 1963
Investigations on Huntington's disease in the Canadian PrairiesM. H. K. Shokeir — 1975
Huntington's diseaseJoseph B. Martin — 1984
OBSERVATIONS ON HUNTINGTON'S CHOREA IN CHILDHOOD.Charles H. Markham, J. William Knox — 1965
Huntington's disease in childrenRandolph K. Byers, Floyd H. Gilles, Christopher Fung — 1973
Juvenile Huntington's choreaPhiroze Hansotia, Charles S. Cleeland, Raymond W. M. Chun — 1968

Cited by

Huntington's disease in children.Derek Letort, Pedro Gonzalez‐Alegre — 2013
A genetic model for age at onset in Huntington disease.Lindsay A. Farrer, P.M. Conneally — 1985
Infantile Bilateral Striatal Necrosis: Clinicopathological ClassificationTakashi Mito — 1986
Huntington's disease of early onset or juvenile Huntington's disease.Neil Gordon — 2003
Predictability of phenotype in Huntington's disease.Lindsay A. Farrer, P.M. Conneally — 1987
Huntington disease in children: genotype-phenotype correlation.Astrid Rasmussen, Rosario Márquez Macías, Petra Yescas — 2000
Clinical Characteristics of Childhood-Onset (Juvenile) Huntington Disease: Report of 12 Patients and Review of the LiteraturePedro Gonzalez‐Alegre, Adel K. Afifi — 2006
Huntington disease: finding the gene and after.John H. Menkes — 1988
Familial Dystonia and Choreoathetosis in Three Generations Associated With Bilateral Striatal NecrosisRandall Craver, M. Caroline Duncan, J. Stuart Nelson — 1996
Juvenile Huntington disease: CT and MR features.Vincent B. Ho, H S Chuang, Miguel J. Rovira — 1995
The Clinical and Genetic Features of Huntington DiseaseAaron Sturrock, Blair R. Leavitt — 2010
Neurodegeneration of the human globus pallidus in Huntington’s diseaseMalvindar K. Singh-Bains — 2014
NEUROPATHOLOGICAL COMPARISON OF ADULT ONSET AND JUVENILE HUNTINGTON’S DISEASE WITH CEREBELLAR ATROPHY: A REPORT OF A FATHER AND SONCaitlin S. Latimer, Margaret E. Flanagan, Patrick J. Cimino — 2017
Clinical Presentation and Features of Juvenile-Onset Huntington’s Disease: A Systematic ReviewThomas Cronin, Anne Rosser, Thomas H. Massey — 2019
Frecuencia De Casos Juveniles Con Enfermedad De Huntington En Población MexicanaVictoria Pérez-González, Eric De-la-Cruz-Estrada, Amin Cervantes‐Arriaga — 2019
Twitches and Fidgets Might Not Tell the Whole StoryM. Robertson, V. Eapen, R. Rizzo — 2016

Related papers

3.18.2 HUNTINGTON'S DISEASE - CLINICAL FEATURES OF PATIENTS WITH HUNTINGTON'S DISEASE INITIALLY DIAGNOSED AS SPINOCEREBELLAR ATAXIAYanhong Dong, Yi‐Min Sun, Zeying Wu — 2012
EXCELLENT ELEMENTS OF PRESENTATION IN BUSINESS ARENAD M Chandravadiya — 2023
Huntington's disease.Ainhi D. Ha, Victor S.C. Fung — 2012
Huntington's disease part 1: what is it?Mark Baker, Daniela Blumlein — 2009
Longitudinal expression changes are weak correlates of disease progression in Huntington’s diseaseChristopher T. Mitchell, Irina Krier, Jamshid Arjomand — 2020
What is the unique nature of the Huntington’s Disease?Adrian Bartoszek, Kamil Szalast — 2019
Controversies and pitfalls in diagnosing Huntington's DiseaseOosterloo Mayke — 2020
Huntington's Disease: The FactsOliver Quarrell — 1999
Impact of Huntington's across the entire disease spectrum: the phases and stages of disease from the patient perspectiveAK Ho, Mevhibe Hocaoğlu, for the European Huntington's Disease Network Quality of Life Working Group — 2011