530 likes | 598 Views
Human Birth Defects. 陳建榮. http://web.nchu.edu.tw/pweb/index2.php?pid=75. Cogenital anomaly 先天性畸形 Teratology 畸胎學. Cause of human congenital anomalies Chromosome 染色体異常 7% – 8% Gene 基因突變 6% – 7% Multifactorial inheritance 多重因子遺傳 7% – 10%
E N D
Human Birth Defects 陳建榮 http://web.nchu.edu.tw/pweb/index2.php?pid=75
Cogenital anomaly先天性畸形 Teratology 畸胎學
Cause of human congenital anomalies Chromosome染色体異常 7% – 8% Gene基因突變 6%– 7% Multifactorial inheritance多重因子遺傳 7% –10% Environmental agents環境因素 20%–25% Unknown未知病因 50%–60%
Anomalies caused by genetic factors: • Numerical chromosome abnormalities • Trisomy of autosomes (table 20-1) • Down syndrom (trisomy of chromosones 21) • Edwards syndrom (trisomy of chromosones 18) • Patau syndrom (trisomy of chromosones 13) • Monosomy X chromosome • Trisomy of sex chromosomes (tabel 20-2) • XXX • XXY • XYY • Terasomy and pentasomy -XXXX, XXXXX, XXXY, XXYY, XXXYY, XXXXY • Triploidy or tetraploidy • Structural chromosome abnormalities
Anomalies caused by genetic factors: • Numerical chromosome abnormalities • Trisomy of autosomes (table 20-1) • Down syndrom (trisomy of chromosones 21) • Edwards syndrom (trisomy of chromosones 18) • Patau syndrom (trisomy of chromosones 13) • Monosomy X chromosome • Trisomy of sex chromosomes (tabel 20-2) • XXX • XXY • XYY • Terasomy and pentasomy -XXXX, XXXXX, XXXY, XXYY, XXXYY, XXXXY • Triploidy or tetraploidy • Structural chromosome abnormalities
Down syndrome (table 20-1) 1. Incidence = 1:800 2. Chromosome 21 3. Incidence & maternal age (table 20-2)
Edwards syndrom (table 20-1) • Incidence = 1:8000 • Chromosome 18
Patau syndrom (table 20-1) • Incidence = 1:25000 • Chromosome 13
Anomalies caused by genetic factors: • Numerical chromosome abnormalities • Trisomy of autosomes (table 20-1) • Down syndrom (trisomy of chromosones 21) • Edwards syndrom (trisomy of chromosones 18) • Patau syndrom (trisomy of chromosones 13) • Monosomy X chromosome • Turner syndrome (X,45) • Trisomy of sex chromosomes (tabel 20-2) • XXX (female, 1:960) • XXY • XYY • Terasomy and pentasomy -XXXX, XXXXX, XXXY, XXYY, XXXYY, XXXXY • Triploidy or tetraploidy • Structural chromosome abnormalities
Turner syndrome (table 20-1) • Incidence =1:8000
Anomalies caused by genetic factors: • Numerical chromosome abnormalities • Trisomy of autosomes (table 20-1) • Down syndrom (trisomy of chromosones 21) • Edwards syndrom (trisomy of chromosones 18) • Patau syndrom (trisomy of chromosones 13) • Monosomy X chromosome • Trisomy of sex chromosomes (tabel 20-2) • XXX (female, 1:960) • XXY • XYY • Terasomy and pentasomy -XXXX, XXXXX, XXXY, XXYY, XXXYY, XXXXY • Triploidy or tetraploidy • Structural chromosome abnormalities
Klinefelter syndrom (XXY) (table 20-3) • Male • Incidence 1:1080 • Small testes, hyalinization of seminiferous tubules (aspermatogenesis)
Anomalies caused by genetic factors: • Numerical chromosome abnormalities • Trisomy of autosomes (table 20-1) • Down syndrom (trisomy of chromosones 21) • Edwards syndrom (trisomy of chromosones 18) • Patau syndrom (trisomy of chromosones 13) • Trisomy of sex chromosomes (tabel 20-2) • XXX (female, 1:960) • XXY • XYY • Terasomy and pentasomy -XXXX, XXXXX, XXXY, XXYY, XXXYY, XXXXY • Triploidy or tetraploidy • Structural chromosome abnormalities
Structural chromosome abnormalities: • Translocation移位 • Deletion削除 • Duplications複製 • Inversion反轉 • Isochromosomes同染色體
Structural chromosome abnormalities Terminal deletion Reciprocal translocation Ring chromosome Paracentric inversion Duplication Robertsonian translocation Isochromosome
Anomalies caused by genetic factors: • Numerical chromosome abnormalities • Trisomy of autosomes (table 20-1) • Turner syndrom (trisomy of chromosones 21) • Edwards syndrom (trisomy of chromosones 18) • Patau syndrom (trisomy of chromosones 13) • Trisomy of sex chromosomes (tabel 20-2) • XXX (female, 1:960) • XXY • XYY • Terasomy and pentasomy -XXXX, XXXXX, XXXY, XXYY, XXXYY, XXXXY • Triploidy or tetraploidy • Structural chromosome abnormalities • Mutant genes
Achondroplasia軟骨發育不全(侏儒症) (Fibroblast) 先天性成骨不全(玻璃娃娃) ALD腎上腺腦白質退化不良症 • X chromosome
Osteogenesis Imperferta先天性成骨不全 Pathogenic changes resulting in osteogenesis imperfecta can occur at any point of collagen synthesis. Beginning with transcription, followed by translation and subsequent posttranslational modification and transport. This figure outlines the basic processes involved in the molecular synthesis of collagen. 1, transcription (most common cause of OI is DNA mutation); 2, translation; 3, CRTAP-P3H1-CycB (CRTAP and P3H1 have recently been identified as causative mechanisms in OI. CRTAP, P3H1, and Cyclophylin B form a complex, which is responsible for the 3-OH of specific COL1 residues) other: prolyl-4-OH; 4, gal transferase/glc transferase; 5, assembly of procollagen chains; 6, disulfide bonds at N terminus; 7, triple helix assembly; 8, protein suicide (after spontaneous triple helix formation, the newly formed microfibril could undergo protein suicide and result in a milder clinical form of OI or the aberrant protein could be included in collagen fibril assembly, where the dominant negative effect results in more severe disease phenotype); 9, secretion; 10, N and C proteinase cleavage of propeptide; 11, collagen fibril assembly.
Anomalies caused by enviromental factors • Teratogens致畸原 (table 20-6) • Critical period of human development • Dosage of the drug or chemical • Genotype of the embryo
Environmental factors • Drugs • Alcohol • Isotretinoin (13-cis-retinoic acid) • Lithium • Phenytoin • Thalidomide • Warfarin • Chemicals • Methylmercury (Minamata bay disease) • PCB (polychlorinated biphenyls) • Infection • CMV, HSV, HIV, Parvovirus B19, Rubella, Varicella, Toxoplasmosis, Syphilis • Radiation (vs Electromagnetic field, Ultrasound) • * > 25000 millirads: harmful to CNS • * diagnostic level: no conclusive proof • chest 1 millirad • pelvis 0.3 – 2 rad • * upper limit of maternal exposure 500 millirad • * embryo exposure < 5rad: minuscule • Maternal factor • DM, PKU • Mechanical factors
Masculinized external genitalia外生殖器男性化 European Mole鼴鼠
Hydantoin syndrome內醯胺症候群 Anticonvulsants 抗痙攣藥 • Trimethadione • Phenytoin
Tranquilizers 鎭靜劑 • Thalidomide沙利竇邁 抗生素 抗凝血劑 止吐藥 抗腫瘤藥 皮質類固醇 鉀鹽……..
E21 day Intraembryonic mesoderm Extraembryonic mesoderm
胸壁、腹壁 Dorsal mesentery 背側腸系膜 Dorsal mesentery: • Intraembryonic mesoderm • Extraembryonic mesoderm
Mesenteries: • Derived from intra- and extra-embryonic mesoderm -Dorsal mesentery -Foregut, midgut, hindgut -greater omentum, mesentery, mesocolon… • Ventral mesentery • Foregut • Lessor omentum, falciform lig., coronary lig….
Division of embryonic body cavity 心包腹膜管 橫中膈 Embryonic cavities: • Pleura cavity • Pericardial cavity • Peritoneal cavity
Pleura and pericardial cavities formation 胸膜心包褶 胸膜心包膜 纖維性心包膜
E24 day E41 day E52 day
Cogenical diaphragmatic hernia先天性橫膈疝氣 Polyhydramnions羊水過多 Left-side defects