Biomedical subjects

U Selldén

Publications and source records attributed to U Selldén.

14 recordsLinked to original sources

PubMed1988

Muscle function and morphology in myotonic dystrophy.

Patients with myotonic dystrophy classified clinically into function groups were studied. Muscle strength for knee extension and flexion was, with few exceptions, moderately or markedly reduced with successively more severe clinical disability. The reduction in maximal walking speed showed a similar tendency. There was a large percentage of both type I and in relation to normal findings of type II C fibers in biopsies from most patients. The fiber area varied greatly even in the patients in the best function groups, some of whom had large type II fibers. The most common-histopathological changes, found in all function groups, were fiber atrophy with small angular fibers, internal nuclei, splitting, fibrosis and moth-eaten fibers. A high percentage of type I fibers can already be seen in patients with practically no other morphological changes and without significant functional deterioration.

Adult↗

PubMed1986

Myotonic dystrophy treated with selenium and vitamin E.

We have previously reported the successful treatment of a patient with myotonic dystrophy with selenium and vitamin E. This paper deals with the treatment of a further five patients with myotonic dystrophy in different stages. All five patients improved subjectively and objectively in two or more respects. All improved their grip strength according to vigorimeter measurements (Martin), two normalized their gait, another two can now sit down on their heels and stand up, one patient can now walk on his toes, one can now get up from lying on the floor without using a chair and two patients have improved their physical capacity. Patients in early stages of the disease improved faster and more markedly than those in late stages. Electromyographical measurements also showed improvements, in that the myotonic discharges had diminished. The daily dose was 4 mg of Na2SeO3 and 600 mg of vitamin E. Serum concentration of selenium increased in all patients at the beginning of the treatment, but stabilized at a level slightly above the normal. No side-effects were observed.

Adult↗

PubMed1983

Hereditary motor and sensory neuropathies in Swedish children. III. De- and remyelinating type in 10 sporadic cases.

Clinical, neurophysiological and certain other laboratory data are given for 10 children considered to represent sporadic cases of de- and remyelinating hereditary motor and sensory neuropathies (HMSN). In all 10 families the parents had been found to be non-affected and said to be non-consanguineous. Nine of the 10 families originated from the two most northerly Swedish counties, but none from the Gothenburg area. The median age at clinical onset was 3 years. Gait abnormalities and/or foot deformities were common reasons for referral. Scoliosis developed in all 10 and hand atrophies in 7 children. In the majority there was neurological deterioration through childhood. Nerve conduction velocities, both motor and sensory, were consistently and markedly reduced. The protein level in cerebrospinal fluid (medium 657 mg/l) was slightly to moderately raised in 7 of 9 examined children and greater than or equal to 1 500 mg/l in the remaining two. The fatty acid pattern of serum lecithin was consistently normal in all 10.

Adolescent↗

PubMed1983

Hereditary motor and sensory neuropathies in Swedish children. II. Neuronal-axonal types.

Clinical, neurophysiological and laboratory data are given for 32 children (30 kinships) considered to represent hereditary motor and sensory neurophaties (HMSN) of neuronal-axonal types. In 25 families (27 cases) one of the parents was found to be affected. In one both parents were normal. The mode of inheritance in the 27 patients with familial neuronal-axonal HMSN was concluded to be autosomal dominant HMSN II (Lambert type). The disability was mild to moderate and, on an average, less pronounced than in de- and remyelinating types of HMSN. Seven out of 27 were early toe-walkers of the secondary type. Cavus feet were noted in 25, hand atrophies in eight and mild scoliosis in five. Sensory complaints were recorded in 21. The nerve conduction velocities (NCVm and NCVs) of children and parents were slightly subnormal in a few. EMG proved to be the most important parameter for identifying subclinically affected parents.

Axons↗

PubMed1980

Nerve conduction velocity in patients with adolescent idiopathic scoliosis.

Measurements of nerve conduction velocity (NCV) in the peroneal and median nerves have been performed in 47 patients with adolescent idiopathic scoliosis (AIS). The results did not reveal any pathology neither asymmetries correlated to convexity of scoliosis. Patients requiring treatment showed significantly lower sensory nerve conduction velocity of median nerve than those under observation. All values, however, were within normal limits. The findings gave no support to any theory that polyneuritis or polyneuropathy is involved in AIS.

Adolescent↗

PubMed1979

Psychiatric assessment of healthy children with various EEG patterns.

A sample of 222 health children, 112 girls and 110 boys, aged 5--16 years, with different types of EEG pattern, were investigated by current child-psychiatric methods. The children were recruited from a large material of children selected in accordance with strict criteria of normality from the paediatric and neurological points of view (Petersén & Eeg-Olofsson (1970/71)). The aim of the child-psychiatric assessment was to find out whether any clinical correlation with the EEG patterns could be shown. First of all, 96 children with some form of EEG deviation were included. Besides these, 126 children with normal EEG were recruited at random from the material. In this selected material significant relations emerged between clinical variables and EEG patterns. Normal EEG showed negative correlations with child-psychiatric variables, while deviating EEG patterns were positively correlated. Many of the correlations disappeared in the oldest age group.

Adolescent↗

PubMed1979

Electroencephalographic investigation of patients with adolescent idiopathic scoliosis.

An EEG study was carried out on 57 children, aged 10--16 years, with idiopathic scoliosis. Treatment (brace or surgery) was required in 37 cases; 20 were being observed only. Controls were 10- to 16-year-old healthy children meeting well-defined criteria of normality. Thirty-four of the scoliotics fulfilled these criteria, thus providing a group matching the controls except for the presence of scoliosis. Thus, any differences occurring could, with reasonable probability, be referred to the disease in question. The comparison with healthy children showed a generally greater EEG pathology in the scoliotics. This was the case in all patients, even those meeting the same criteria of normality as the controls. A highly significant difference was noted in the occurrence of paroxysmal activity. Type and localization of abnormally (bilaterally synchronous discharges) indicated involvement of subcortical structures. Comparison within the scoliotic group showed that EEG abnormalities were not correlated with the magnitude of the disease except for the variable "paroxysmal activity at rest". Patients submitted to observation only presented paroxysmal activity significantly more often than patients requiring treatment. The localization of abnormality within the hemispheres did not agree or disagree systematically with the convexity of the curve. A possible relationship between the higher incidence of scoliosis in females and the higher sensitivity to afferent stimuli as found in the female EEG is also discussed.

Adolescent↗

PubMed1976

Adverse effects of lumbar myelography with amipaque and dimer-X.

The adverse effects in a series of 50 lumbar myelographies with Amipaque were compared with those in a corresponding series, examined with Dimer-X. Side effects occurred in 58% of the cases examined with Amipaque and in 68% of the Dimer-X series. No seizures occurred in 58% of the cases examined with Amipaque and in 68% of the Dimer-X series. No seizures occurred in either series but slight fibrillations of fasciculations appeared in 2 Dimer-X patients. Hyperreflexia of the legs was recorded in 22% of the Amipaque and in 36% of the Dimer-X cases. Other adverse reactions to the media were mild to moderate. Some burst activity, but no definite paroxysmal abnormality was noted in EEG recordings in 2 Amipaque cases. The low epileptogenicity of Amipaque has ensured a wider safety margin of lumbar myelography.

Adult↗

PubMed1975

Side effects after lumbar myelography with dimeglumine iocarmate (Dimer-X). Further experiences.

Lumbar myelography with dimeglumine iocarmate was performed in 90 cases premedicated with diazepam (Valium). EEG was performed before, as well as 3 and 24 hours after myelography. The use of diazepam interfered to some extent with the interpretation of the EEG. In 3 cases EEG abnormalities occurred 3 hours after myelography, most probably ascribable to Dimer-X. No further changes were found in the 24-hour recording. Immediate side effects were few and mild and seizures did not appear. The EEG abnormalities were equally distributed among patients with and without side effects.

Adolescent↗

PubMed1971