ABSTRACT
Cytogenetic data obtained from investigating 1001 patients of Down syndrome (DS) and their parents over a period of 20 years (January 1979-January 1999) are presented. The frequency of pure trisomy, mosaicism and translocation was 87.92, 7.69 and 4.39 per cent respectively. The origin of the extra chromosome 21 due to meiotic non-disjunction was 79.24 per cent maternal and 20.76 per cent paternal. A high frequency of acrocentric chromosome associations was also observed in mothers of children of Down syndrome, this might have predisposed to an enhanced risk for non-disjunction. Birth order of DS showed a higher number of first and second borns. Reproductive performances of the parents indicated a high rate of abortions, compared to controls. Cytogenetic investigations carried out over these years greatly helped in the management of these children and for counseling the affected families.
Subject(s)
Chromosome Aberrations , Down Syndrome/genetics , Adolescent , Adult , Child , Child, Preschool , Humans , Infant , Infant, Newborn , Mosaicism , Translocation, Genetic , TrisomyABSTRACT
Eight females with a family history of Duchenne muscular dystrophy (DMD) were analysed for their carrier status by m-calpain test, which monitors the m-calpain (milli-calpain), a proteolytic enzyme in the platelets, using an ELISA technique. Four of the eight females were identified as carriers by virtue of their elevated enzyme levels as compared to control. DNA samples of these members were analysed to ascertain the carrier status, by PCR followed by dosage analysis by densitometry. DNA analysis confirmed the findings by calpain test, which underlines the reliability of this phenotypic test for carrier detection in DMD. Calpain test has been informative in a large group of patients and carriers tested so far. Since the calpain test is cost and labour effective, it is suited for routine and widespread screening purposes.
Subject(s)
Calpain/genetics , Muscular Dystrophies/genetics , Blood Platelets/physiology , Enzyme-Linked Immunosorbent Assay , Female , Heterozygote , Humans , Pedigree , Polymerase Chain Reaction , Sequence DeletionABSTRACT
Reproductive history of mothers of 115 Down's syndrome children was studied and compared with 200 control mothers who gave birth to normal children. The frequency of spontaneous abortions in mothers of Down's syndrome babies was found to be elevated significantly (p < 0.05). The data suggest that the maternal health and reproductive potential have a prominent aetiological significance in the occurrence of Down's syndrome.
Subject(s)
Abortion, Spontaneous/etiology , Down Syndrome/etiology , Reproductive History , Case-Control Studies , Down Syndrome/genetics , Female , Humans , Karyotyping , Mosaicism , Pregnancy , TrisomyABSTRACT
Peripheral blood lymphocyte cultures of 116 smokers and 80 non-smokers who were occupationally exposed to uranyl compounds were analysed for sister-chromatid exchanges (SCEs). Blood samples were collected from 59 non-smokers (control group I) and 47 smokers (control group II) who were not exposed to uranium for control data. A significant increase in SCEs was observed among both smokers and non-smokers exposed to uranyl compounds when compared to their respective controls. In controls, a significant increase in the frequency of SCEs was observed in smokers when compared to non-smokers.
Subject(s)
Mutagens/toxicity , Occupational Exposure , Power Plants , Sister Chromatid Exchange , Uranium Compounds/toxicity , Adult , Female , Humans , Lymphocytes/radiation effects , Male , Middle Aged , Smoking/adverse effectsABSTRACT
Calcium and calcium dependent enzymes viz., calcium ATPase, protein kinase C and calcium activated neutral protease (milli CANP mCANP) were studied in the erythrocytes, platelets and lymphocytes of obligate carriers, in order to assess the usefulness of these indices for detection of carriers for Duchenne muscular dystrophy (DMD). With the exception of mCANP and lymphocyte calcium ATPase, other calcium dependent enzyme activities showed considerable overlap between carriers and control. Since the increase in the level of platelet mCANP was found in all affected boys (no false negatives) and obligate carriers, and patients with other myopathic conditions and some neurogenic causes did not show high platelet mCANP activity, this parameter could be considered as a good phenotypic index. Unlike SCK, the platelet mCANP of carriers did not overlap that of controls, hence tests are to be carried out to verify its usefulness as an index of carrier state in mutations other than DNA deletion since testing of non-deletion is both costly and has practical limitations.
Subject(s)
Calcium-Transporting ATPases/blood , Calcium/blood , Calpain/blood , Heterozygote , Muscular Dystrophies/genetics , Protein Kinase C/blood , Adult , Erythrocytes/chemistry , Humans , MaleABSTRACT
A total of 118 cases of microcephaly were clinically evaluated under two main groups: primary microcephaly (61 cases) and secondary microcephaly (57 cases). Secondary cases were generally characterized by convulsions, spasticity, and other congenital anomalies. Estimates of segregation frequency obtained separately in primary and secondary cases indicated that the primary consanguineous cases were most probably due to a single recessive gene. The segregation frequency was substantially less in other types, indicating much lower genetic risks in these cases.
Subject(s)
Consanguinity , Genes, Recessive , Microcephaly/genetics , Female , Gene Frequency , Humans , India , MaleSubject(s)
Anencephaly/diagnosis , Diseases in Twins , Ultrasonography , Adult , Female , Humans , Pregnancy , Prenatal DiagnosisABSTRACT
Clinical and genetic studies were made on progressive muscular dystrophy in eight young girls. No chromosomal abnormality was observed in these patients and their mothers. The pedigrees of six cases suggested an autosomal recessive inheritance and clinical features were identical with those of Duchenne muscular dystrophy. Two other cases were compatible with childhood muscular dystrophy with autosomal recessive inheritance.
Subject(s)
Muscular Dystrophies/genetics , Consanguinity , Female , Genes, Recessive , Humans , PedigreeSubject(s)
Iris/abnormalities , Adult , Child, Preschool , Humans , India , Infant , Karyotyping , Male , Middle Aged , PedigreeSubject(s)
Genetic Variation , Hemophilia A/genetics , Child, Preschool , Factor VIII/analysis , Female , Hemophilia A/blood , Heterozygote , Humans , Infant , Male , PedigreeSubject(s)
Polycystic Kidney Diseases/diagnosis , Prenatal Diagnosis , Ultrasonography , Adult , Female , Humans , Male , PregnancyABSTRACT
The chewing of betel leaf with other ingredients is a widespread addiction in India. The chromosome damaging effect was studied in human leukocyte cultures. There was an increase in the frequency of chromatid aberrations when the leaf extract was added to cultures.
