| 000 | 02713cam a2200349 a 4500 | ||
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| 003 | EG-GiCUC | ||
| 005 | 20250223031712.0 | ||
| 008 | 170403s2016 ua h f m 000 0 eng d | ||
| 040 |
_aEG-GiCUC _beng _cEG-GiCUC |
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| 041 | 0 | _aeng | |
| 049 | _aDeposite | ||
| 097 | _aPh.D | ||
| 099 | _aCai01.11.07.Ph.D.2016.Ra.A | ||
| 100 | 0 | _aRasha Mohamed Helmy Osman Elkaffas | |
| 245 | 1 | 0 |
_aAssociation of abcc8 and insulin gene mutations with diabetes mellitus in Egyptian neonates and infants in the first year of life / _cRasha Mohamed Helmy Osman Elkaffas ; Supervised Badawy Mohamad Alkholy , Mona Foad Hafez , Hanan Ali Madani |
| 246 | 1 | 5 | _aارتباط طفرات جينى ال اب س س٨ و الانسولين و مرض البول السكرى فى حديثى الولادة و الاطفال المصريين فى عامهم الاول |
| 260 |
_aCairo : _bRasha Mohamed Helmy Osman Elkaffas , _c2016 |
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| 300 |
_a153 P. : _bfacsimiles ; _c25cm |
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| 502 | _aThesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Clinical and Chemical Pathology | ||
| 520 | _aNeonatal diabetes mellitus (NDM) is a monogenic form of diabetes resulting from mutations in a number of different genes encoding proteins that play a key role in the normal function of the pancreatic beta-cell. Mutations in the genes encoding the ATP-sensitive potassium channel [(potassium inwardly rectifying channel, subfamily J, member11 (KCNJ11) and ATP-binding cassette transporter subfamily C, member 8 (ABCC8)] and the insulin (INS) genes are the commonest causes of the NDM. The identification of these mutations by genetic test»ing is critical for appropriate management and to guide genetic counseling. This study aimed to determine ABCC8 and IN genes mutations in a group of Egyptian diabetic neonates and infants under the age of 1 year and to determine other candidate genetic causes of NDM according to the patient{u2019}s clinical phenotype. DNA sequencing of the coding regions and intronic boundaries of ABCC8 and INS genes was done in 25 patients. Further candidate genes sequencing according to the clinical phenotype was done. Two patients (10%) had three ABCC8 mutations in the form of a compound heterozygous (p.N131K/p.R598*) in one patient and a homozygous (p.R1554Q) in the other patient | ||
| 530 | _aIssued also as CD | ||
| 653 | 4 | _aABCC8 | |
| 653 | 4 | _aDiabetes mellitus | |
| 653 | 4 | _aInsulin gene mutations | |
| 700 | 0 |
_aBadawy Mohamad Alkholy , _eSupervisor |
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| 700 | 0 |
_aHanan Ali Madani , _eSupervisor |
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| 700 | 0 |
_aMona Foad Hafez , _eSupervisor |
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| 856 | _uhttp://172.23.153.220/th.pdf | ||
| 905 |
_aNazla _eRevisor |
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| 905 |
_aSamia _eCataloger |
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| 942 |
_2ddc _cTH |
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| 999 |
_c60524 _d60524 |
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