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1.
Eur J Oral Sci ; 115(4): 308-14, 2007 Aug.
Article in English | MEDLINE | ID: mdl-17697171

ABSTRACT

In order to assess whether naturally occurring oral lactobacilli have probiotic properties, lactobacilli were isolated from saliva and plaque from children and adolescents, with or without caries lesions. The interference capacities of these lactobacilli were investigated against a panel of 13 clinical isolates and reference strains of Streptococcus mutans and Streptococcus sobrinus, as well as against the subject's autologous mutans streptococci, using the agar-overlay technique. Lactobacillus-mediated inhibition differed significantly between the three subject groups (no caries, arrested caries, or active caries), demonstrating increased inhibition in subjects without present or previous caries experience compared to subjects with arrested caries or subjects presenting with frank lesions. Lactobacilli from subjects lacking S. mutans inhibited the growth of the test panel of mutans streptococci significantly better than lactobacilli from subjects who were colonized. Furthermore, subjects without caries experience harbored lactobacilli that more effectively repressed the growth of their autologous mutans streptococci. Twenty-three Lactobacillus spp. completely inhibited the growth of all mutans streptococci tested. Species with maximum interference capacity against mutans streptococci included Lactobacillus paracasei, Lactobacillus plantarum, and Lactobacillus rhamnosus. Naturally occurring oral lactobacilli significantly inhibited the growth of both test strains of mutans streptococci and the subject's autologous mutans streptococci in vitro, and this effect was more pronounced in caries-free subjects.


Subject(s)
Antibiosis/physiology , Dental Caries/microbiology , Dental Plaque/microbiology , Lactobacillus/physiology , Saliva/microbiology , Streptococcus mutans/growth & development , Adolescent , Adult , Child , Dental Caries/diagnostic imaging , Female , Humans , Male , Radiography , Single-Blind Method , Species Specificity
2.
Am J Med Genet A ; 143A(12): 1317-25, 2007 Jun 15.
Article in English | MEDLINE | ID: mdl-17506093

ABSTRACT

Swedish patients with the oculo-auriculo-vertebral (OAV) spectrum participated in a prospective multidisciplinary investigation. The aims of the study were to describe their systemic and functional defects, especially autism spectrum disorders, and to search for possible etiologic risk factors. Available medical records were studied and the mothers answered a questionnaire on history of prenatal events. A clinical examination evaluating systemic findings, vision, hearing, speech, oral and swallowing function, and neuropsychiatric function, especially autism, was made. Eighteen patients, (11 males, 7 females) aged 8 months to 17 years with OAV were studied. Most frequent systemic malformations included, ear abnormalities (100%), ocular malformations (72%), vertebral deformities (67%), cerebral anomalies (50%), and congenital heart defects (33%). Functional defects consisted of hearing impairment (83%), visual impairment (28%), both visual and hearing impairment (28%), difficulties in feeding/eating (50%), speech (53%), mental retardation (39%), and severe autistic symptoms (11%). Three children were born following assisted fertilization (two intracytoplasmatic sperm injection, one in vitro fertilization), two mothers reported early bleedings, and six (33%) mothers had smoked during pregnancy.


Subject(s)
Feeding and Eating Disorders/pathology , Goldenhar Syndrome/pathology , Intellectual Disability/pathology , Sensation Disorders/pathology , Speech Disorders/pathology , Adolescent , Cerebrum/abnormalities , Child , Child, Preschool , Ear/abnormalities , Eye Abnormalities/pathology , Female , Goldenhar Syndrome/genetics , Heart Defects, Congenital/pathology , Humans , Infant , Male , Neuropsychological Tests , Prospective Studies , Risk Factors , Spine/abnormalities , Sweden
3.
Am J Med Genet A ; 133A(3): 331-9, 2005 Mar 15.
Article in English | MEDLINE | ID: mdl-15633180

ABSTRACT

CHARGE association (CA) consists of a non-random association of ocular coloboma (C), heart anomaly (H), atresia of choanae (A), retarded growth and/or development (R), genital hypoplasia (G), and ear anomalies and/or hearing impairment (E). A prospective multidisciplinary study of 31 Swedish patients with CA was undertaken in order to describe the associated malformations and functional deficits, find possible etiological factors and identify critical time periods for the maldevelopment. The clinical files were analyzed, the mothers answered a questionnaire on history of prenatal events, and a clinical evaluation of systemic findings, vision, hearing, balance, speech, oral and swallowing function, and neuro-psychiatric function, especially autism, was performed. The most frequent physical abnormalities affected ears (90%), eyes (90%), brain (61%), heart (52%), retarded growth (48%), genitals (38%), choanae (35%), and facial nerve (32%). Sixty-one percent of the patients were visually impaired or blind, and 74% had hearing loss or deafness. Problems in balance, speech, and eating were common. Forty percent of the patients had autism/atypical autism, and 82% had developmental delay. Three children were born following assisted fertilization and two mothers had diabetes. The mothers reported infections, bleedings, and drug use during pregnancy. Analysis of possible critical time periods suggested that most malformations were produced early in pregnancy, mainly during post conceptual weeks 4, 5, and 6. A multidisciplinary approach is essential in the assessment and management of CA.


Subject(s)
Abnormalities, Multiple/pathology , Choanal Atresia/pathology , Coloboma/pathology , Heart Defects, Congenital/pathology , Abnormalities, Multiple/etiology , Abnormalities, Multiple/physiopathology , Adolescent , Adult , Autistic Disorder/pathology , Autistic Disorder/physiopathology , Child , Child, Preschool , Deafness/pathology , Ear/abnormalities , Female , Genitalia/abnormalities , Growth Disorders/pathology , Humans , Infant , Infant, Newborn , Male , Maternal Age , Paternal Age , Risk Factors , Sweden , Syndrome
4.
Eur J Paediatr Neurol ; 6(1): 35-45, 2002.
Article in English | MEDLINE | ID: mdl-11993954

ABSTRACT

Mobius sequence/syndrome is a rare disorder characterized by congenital palsy of the 6th and 7th cranial nerves. Other cranial nerves may be affected, skeletal and orofacial anomalies and mental retardation occur. The aims were to determine the frequency of associated clinical characteristics and to identify any pregnancy or environmental factors in patients with Mobius sequence. A prospective study of 25 Swedes with apparent involvement of the 6th and 7th cranial nerves was performed and 25 patients, 1 month to 55 years old, were examined. Obvious associated systemic anomalies observed included: limb malformations (10), Poland anomaly (2), hypodontia (7), microglossia (6), cleft palate (4), hearing impairment (5) and external ear malformation (1). Pronounced functional abnormalities were observed involving facial expression (16), speech (13), eating and swallowing (12) and difficulty in sucking in infancy (11). Six patients had an autistic syndrome, one an autistic-like condition, and mental retardation was found in all these patients. No common aetiological cause was found but their mothers' pregnancy histories revealed a history of benzodiazepines (1), bleeding during pregnancy (8), spontaneous abortion (7) and chorion villus sampling in the second month of pregnancy (1). In conclusion, many patients had multiple problems with eating and communication resulting from facial palsy, cleft palate and tongue anomalies. Autism and mental retardation was diagnosed in one-third of the patients. Awareness of the wide spectrum of manifestations in Mobius sequence will assist in identification of the associated malformations and functional problems that are often seen and result in better care of the children.


Subject(s)
Mobius Syndrome/physiopathology , Patient Care Team , Abducens Nerve Diseases/complications , Abducens Nerve Diseases/physiopathology , Adolescent , Adult , Autistic Disorder/complications , Child , Child, Preschool , Facial Paralysis/complications , Facial Paralysis/physiopathology , Female , Follow-Up Studies , Foot Deformities/complications , Gestational Age , Hand Deformities/complications , Humans , Hypoglossal Nerve Diseases/complications , Hypoglossal Nerve Diseases/physiopathology , Infant , Infant, Newborn , Intellectual Disability/complications , Male , Middle Aged , Mobius Syndrome/diagnosis
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