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1.
Ned Tijdschr Geneeskd ; 150(48): 2625-9, 2006 Dec 02.
Article in Dutch | MEDLINE | ID: mdl-17205936

ABSTRACT

Three healthy boys, 3.5, 5 and 1.5 years of age, were admitted to hospital with a severe bacterial skin infection, cerebellar ataxia, and pneumonia, respectively, one week after the onset of varicella. They recovered completely after treatment. Studies in Europe report complications from varicella in 2.5% of healthy children. Most of these are neurological complications and secondary bacterial infections of skin and soft tissue. Last year, a European consensus was published that recommended that all healthy children be vaccinated against chickenpox. In The Netherlands, routine varicella zoster virus (VZV) vaccination has not (yet) been implemented. We propose a new discussion on the possible inclusion of VZV vaccination in the national vaccination programme.


Subject(s)
Cerebellar Ataxia/etiology , Chickenpox Vaccine , Chickenpox/complications , Herpesvirus 3, Human/immunology , Pleuropneumonia/etiology , Skin Diseases, Bacterial/etiology , Cerebellar Ataxia/epidemiology , Chickenpox/prevention & control , Child, Preschool , Health Policy , Humans , Immunization Programs , Infant , Male , Netherlands/epidemiology , Pleuropneumonia/epidemiology , Skin Diseases, Bacterial/epidemiology
2.
Ned Tijdschr Geneeskd ; 149(2): 89-92, 2005 Jan 08.
Article in Dutch | MEDLINE | ID: mdl-15688841

ABSTRACT

A 14-year-old girl with Graves' disease developed a fever, sore throat and a severe systemic infection after being treated with antithyroid drugs for 1 year. Agranulocytosis was diagnosed. After long-term antibiotic treatment and supportive therapy she recovered. Agranulocytosis is a known side-effect of antithyroid drugs and is seen in 0.2 to 0.5% of the patients. It usually occurs within the first 3 months of treatment. Patients above the age of 40 seem to be more susceptible. Since the onset of agranulocytosis is relatively acute, routine blood monitoring is not very useful. It is more important to instruct patients who use a thyreostatic to contact their physician in case of unexplained fever or a sore throat.


Subject(s)
Agranulocytosis/chemically induced , Anti-Bacterial Agents/therapeutic use , Antithyroid Agents/adverse effects , Adolescent , Agranulocytosis/drug therapy , Female , Fever/chemically induced , Graves Disease/drug therapy , Humans , Pharyngitis/chemically induced , Treatment Outcome
3.
Clin Genet ; 53(1): 74-8, 1998 Jan.
Article in English | MEDLINE | ID: mdl-9550367

ABSTRACT

This paper describes a patient with a de novo inverted duplication of chromosome 8(q13-q21.2). He was born with a ventricular septum defect, glandular hypospadias and protruding ears. At the age of 5 1/2 years he had normal psychomotor development. Review of the literature on partial duplications of 8q reveals that the associated phenotype may be mild. Normal psychomotor development, as in our patient, however appears to be uncommon.


Subject(s)
Abnormalities, Multiple/genetics , Chromosome Inversion , Chromosomes, Human, Pair 8 , Heart Septal Defects, Ventricular/genetics , Hypospadias/genetics , Child, Preschool , Humans , In Situ Hybridization, Fluorescence , Karyotyping , Male
4.
Ned Tijdschr Geneeskd ; 141(8): 385-7, 1997 Feb 22.
Article in Dutch | MEDLINE | ID: mdl-9157299

ABSTRACT

In 2 boys aged 8 years and 10 months, respectively, uncommon manifestations of cat scratch disease were seen. The first patient had acute encephalopathy: coma and generalized tonic-clinic convulsions. The second patient was presented with fever and peripheral lymphadenopathy in combination with hypodense lesions in the liver on ultrasound. Diagnosis was established on the clinical picture and the positive results of serological testing of antibody titres for Bartonella henselae. Both patients recovered completely within 2 months.


Subject(s)
Bartonella henselae , Cat-Scratch Disease/complications , Encephalitis/etiology , Antibodies, Bacterial/isolation & purification , Bartonella henselae/immunology , Cat-Scratch Disease/microbiology , Child , Coma/etiology , Encephalitis/microbiology , Hepatitis/etiology , Hepatitis/microbiology , Humans , Infant , Lymphadenitis/etiology , Lymphadenitis/microbiology , Male
5.
Ned Tijdschr Geneeskd ; 138(44): 2204-7, 1994 Oct 29.
Article in Dutch | MEDLINE | ID: mdl-7969601

ABSTRACT

The Netherlands Centre for Monitoring of Adverse Reactions to Drugs received two reports of adrenal suppression, attributed to inhaled budesonide. In the first patient, a 7-year-old girl, there were growth retardation, centripetal weight gain and a Cushingoid moonface with unmeasurable serum levels of cortisol after long-term treatment with 600, and later 1000 micrograms daily. In the second patient, an 8-year-old boy, there was malaise with onset a few months after start of treatment with 400 micrograms budesonide daily. There was a lowered serum level of cortisol which returned to normal after discontinuation of budesonide. Although inhaled corticosteroids cause systemic adverse effects less frequently than orally administered corticosteroids, such effects may occur occasionally.


Subject(s)
Adrenal Insufficiency/chemically induced , Bronchodilator Agents/adverse effects , Pregnenediones/adverse effects , Administration, Topical , Adrenal Cortex/drug effects , Aerosols , Anti-Inflammatory Agents/adverse effects , Asthma/drug therapy , Budesonide , Child , Cushing Syndrome/chemically induced , Female , Glucocorticoids/adverse effects , Humans , Male , Pregnenediones/therapeutic use
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