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1.
Asian Pac J Allergy Immunol ; 37(1): 1-8, 2019 Mar.
Article in English | MEDLINE | ID: mdl-29223147

ABSTRACT

INTRODUCTION: There is a high and rising prevalence of many allergic diseases in the Asia Pacific, including Hong Kong (HK), which is unmatched by a commensurate provision of clinical allergy services. METHOD: This review highlights progress and deficiencies in allergy service and training in HK. The allergy work force was estimated from the numbers of doctors practicing allergy registered with the HK Medical Council Specialist Register in Immunology and Allergy; Paediatric Immunology and Infectious Diseases (includes allergy); Paediatrics; and Immunology (as a discipline of Pathology). The numbers of trainees were estimated from the trainee lists of the Hong Kong Colleges of Physicians, Paediatrics and Pathology. The numbers of allergy clinics were estimated from existing services in Hospital Authority public hospitals in HK. RESULTS: In the last 3 years, two new drug allergy clinics have been established in public hospitals, and for the first time in 20 years, Hong Kong has a trainee in adult allergy. The current ratio of allergists per head of population has improved slightly from 1:1.46 million in 2014 to 1:1.17 million, but it is still low compared to many countries. There are 5-fold more paediatric allergists than adult allergists per head of population in HK. DISCUSSION: Hong Kong is not equipped to take advantage of major public health advances in allergy prevention. If the unbalance of adult to paediatric allergists remains uncorrected, continuing care for allergic children as they grow into adulthood will be an increasing problem. CONCLUSION: Hong Kong still has an unmet need for allergy specialists and is ill equipped to exploit recently discovered public health opportunities to prevent allergy. This review provides recommendations to improve allergy service provision and training, including the creation of Centres of Excellence in allergy to drive the growth of the specialty.


Subject(s)
Health Services , Hypersensitivity/epidemiology , Hypersensitivity/prevention & control , Education, Medical , Health Resources , Health Services/standards , Health Workforce , Hong Kong/epidemiology , Humans , Public Health Surveillance
2.
Am J Med Genet A ; 120A(3): 413-7, 2003 Jul 30.
Article in English | MEDLINE | ID: mdl-12838565

ABSTRACT

Interstitial deletions of the long arm of chromosome 3 are uncommon. Most cases are related to the blepharophimosis-ptosis-epicanthus inversus syndrome (BPES), which is mapped to 3q23. We report on a case with a de novo chromosomal deletion of 3q23 and 3q25. We review the literature on the reported cases of 3q deletion and find that the condition of our patient is not typical of the BPES. Rather, she shares similarity to a patient with Wisconsin syndrome, first discovered in 1976.


Subject(s)
Chromosome Deletion , Chromosome Disorders/physiopathology , Chromosomes, Human, Pair 3 , Abnormalities, Multiple/genetics , Abnormalities, Multiple/physiopathology , Adolescent , Child , Child, Preschool , Chromosome Disorders/genetics , Craniofacial Abnormalities/genetics , Craniofacial Abnormalities/physiopathology , Developmental Disabilities/genetics , Developmental Disabilities/physiopathology , Female , Humans , In Situ Hybridization, Fluorescence , Infant
3.
Chin Med J (Engl) ; 115(4): 607-11, 2002 Apr.
Article in English | MEDLINE | ID: mdl-12133309

ABSTRACT

OBJECTIVE: To establish a profile of the causes of apparently unexplained SS in genetic referral center and evaluate the current referral system. METHODS: This was a retrospective database survey on patients who were referred our clinical genetic service from 1988 - 1998 primarily because of SS. We retrieved the study population from our computer database using "short stature"as a search handle and then studied the demographic, clinical and laboratory data from their medical records. RESULTS: Three hundred and fifty-three subjects were referred for genetic evaluation of SS in 1988 - 1998. The mean age of referred subjects was 11.5 years and the female to male ratio was 7.6. All referrals had undergone cytogenetic studies to exclude chromosomal abnormalities, 19% of girls with apparently unexplained short stature had Turner syndrome; at least 47.9% of the study population were normal variants and 25% of the referrals had inadequate information for classification. CONCLUSIONS: Genetic investigation is essential in the management of patients with SS, especially for girls suspected of having Turner syndrome, in which growth hormone treatment has shown to improve final height. We also highlight the inherited causes of short stature, which were often misdiagnosed as benign familial short stature, and discussed the drawbacks of the current referral system.


Subject(s)
Growth Disorders/genetics , Referral and Consultation/statistics & numerical data , Child , Databases as Topic/statistics & numerical data , Family Health , Female , Growth Disorders/diagnosis , Growth Disorders/epidemiology , Hong Kong/epidemiology , Humans , Karyotyping , Male , Retrospective Studies , Turner Syndrome/genetics
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