This document discusses a genetic condition where about 1 in 50,000 newborns are affected. Symptoms include a high-pitched cry, downward slanted eyes, low birth weight, intellectual disability, webbed fingers or toes, and other physical abnormalities. Doctors focus on managing individual symptoms rather than curing the underlying genetic cause.
Cri du chat syndrome, also known as chromosome 5p deletion syndrome, 5p (said minus) syndrome or Lejeunes syndrome, is a rare genetic disorder due to a missing part (deletion) of chromosome 5.[1] Its name is a French term (cat-cry or call of the cat) referring to the characteristic cat-like cry of affected children.[2] It was first described by J辿r担me Lejeune in 1963.
This document discusses a genetic condition where about 1 in 50,000 newborns are affected. Symptoms include a high-pitched cry, downward slanted eyes, low birth weight, intellectual disability, webbed fingers or toes, and other physical abnormalities. Doctors focus on managing individual symptoms rather than curing the underlying genetic cause.
Cri du chat syndrome, also known as chromosome 5p deletion syndrome, 5p (said minus) syndrome or Lejeunes syndrome, is a rare genetic disorder due to a missing part (deletion) of chromosome 5.[1] Its name is a French term (cat-cry or call of the cat) referring to the characteristic cat-like cry of affected children.[2] It was first described by J辿r担me Lejeune in 1963.
Cri-du-chat syndrome, also known as chromosome 5p deletion syndrome, is caused by a deletion on the short arm of chromosome 5. It is characterized by a cat-like cry in affected infants due to problems with larynx development. Other symptoms include small size, mental retardation, small head and jaw, distinctive facial features and limb abnormalities. While there is no cure, treatment focuses on managing symptoms through physical and speech therapy. The condition occurs in approximately 1 in 20,000 to 50,000 live births.
Cri du chat syndrome is a rare genetic disorder caused by a missing part of chromosome 5, affecting an estimated 1 in 20,000 to 50,000 live births. It is usually not inherited from parents and more commonly found in females. While the condition cannot be cured, symptoms such as feeding issues and speech delays can be treated through early therapy. Parents are also advised to seek counseling.
Turner syndrome is a genetic condition that affects females, caused by missing or structural abnormalities of an X chromosome. It can cause short stature, lack of sexual development at puberty, infertility, and other health issues. Klinefelter syndrome is a condition in males caused by at least one extra X chromosome, resulting in enlarged breasts and reduced facial/body hair. Fragile X syndrome is caused by a gene on the X chromosome shutting down, leading to intellectual disabilities, large ears, joint issues, and other traits.
Kline Felter Syndrome is a genetic disorder where males are born with an extra X chromosome, resulting in XXY sex chromosomes. It occurs due to a random error in the mother and father's sex cells when the baby is conceived. Signs include a taller and less muscular body type, broader hips, larger breasts, weaker bones, and smaller genitals. It can cause learning problems and issues with sexual development or infertility. While there is no cure, treatments can help address symptoms.
Mutasi Kromosom pelajaran kelas XII SMA
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semoga bermanfaat terutama untuk seluruh kelas XII SMA yang akan menghadapi UN!!!
The chromosomal finding was triploidy 69,XXY. Triploidy occurs when a fetus has three full sets of chromosomes instead of the normal two and results in lethality during prenatal development. Numerical chromosomal abnormalities include polyploidy, aneuploidy, and nullisomy/disomy in gametes which can cause conditions like Down syndrome (trisomy 21), Patau syndrome (trisomy 13), Edwards syndrome (trisomy 18), Turner syndrome (monosomy X), and Klinefelter syndrome (47,XXY).
This presentation is fetures the basic introduction to Genome mosaicism in humans and nature, with some examples of its harmful effects on humans, with
2. Sindromul Klinefelter (XXY)
Apare la brba釘i
Prezint corpuscul
Barr
Pilozitate redus
Dispunerea 釘esutului
adipos de tip feminin
Ginecomastie
Criptorhidie 樽nso釘it de
sterilitate
Afec釘iuni psihice
3. Cariotipul unui brbat cu sindromul
Klinefelter
ACEASTA TULBURARE
GENETICA SE
DATOREAZA PREZENTEI
IN PLUS A
CROMOZOMILOR X
FATA DE NORMAL.
5. V-ati intrebat de ce unii
baieti sau barbati au o
musculatura slab
dezvoltata, bazinul mai lat,
umerii ingusti, picioarele
mai lungi, inaltimea mai
mare decat ceilalti de varsta
lor si de multe ori prezinta
semne de feminitate? Ei
bine, ei sufera de sindromul
Klinefelter, o boala genetica
care apare numai la barbati.
7. De regula un barbat are un cromozom Y si
unul X, insa in cazul in care sufera de
sindromul Klinefelter va mai avea unul sau mai
multi astfel de cromozomi X. Incidenta acestei
boli in randul populatiei este destul de mica, s-
a stabilit ca doar un barbat din 600 sufera de
acest sindrom.
8. CAUZELE SINDROMULUI KLINEFELTER
In majoritatea cazurilor sindromul
Klinefelter se datoreaza unei erori
ce apare in procesul diviziunii
celulare si anume: dupa ce
spermatozoidul fecundeaza ovulul
apare un cromozom X in plus.
9. SIMPTOMELE SINDROMUL
KLINEFELTER
Boala se caracterizeaza prin mai
multe schimbari marcante la nivelul
corpului. Principalele simptome ale
bolii apar dupa pubertate. La 50 %
din pacienti s-a remarcat o crestere a
sanilor, numita ginecomastie.
Musculatura este slab dezvoltata.
10. Pilozitatea faciala si pubiana este scazuta. Persoana in
cauza prezinta o hipertrofie a glandelor mamare (asa
numita ginecomastie).
Are picioarele mai lungi, bazinul mai lat si umerii mai
ingusti decat in mod normal.
Prezinta o scadere a apetitului sexual, are texticulele
mai mici decat ar trebui la varsta respectiva.
In majoritatea cazurilor un astfel de pacient poate fi
infertil si necesita metode speciale de fertilizare. Are
penisul mic si testiculele subdezvoltate.
11. Ii este afectata dezvoltarea intelectuala, are
probleme de comunicare, de exprimare, de
rezolvare a unei situatii si de intocmire a unui
plan de actiune.
Vocabularul sau este sarac, procesul de
gandire incetinit, isi controleaza impulsurile
mai greu. Are probleme de integrare sociala
inca din anii de scoala.
12. Bolnavul poate manifesta anumite patologii
osoase si anume: curburi ale oaselor de la
degete, deformari ale oaselor in zona pieptului, a
partii superioare a bratului sau la coapse. In
anumite cazuri apar tumori si malformatii
cardiace.
Dintre toate aceste simptome cea mai grava
complicatie este infertilitatea. Acel cromozom X
care este in plus poate afecta testiculele sau
gonadele masculine si astfel reduce productia de
sperma.
13. Sindromul Klinefelter se poate depista prin
amniocenteza la femeia gravida sau prin
biopsia vilozitatilor cronice. Daca se banuieste
un astfel de sindrom, pana la varsta adulta se
poate efectua testul cariotip ce permite
descoperirea unor anomalii ale cromozomilor.
Analiza spermei si dozarile hormonale sunt
teste de laborator care pot duce la
diagnosticarea bolii de catre un medic
specialist.
14. PRINCIPALELE METODE DE TRATAMENT IN
CAZUL SINDROMUL KLINEFELTER:
Cel mai important tratament in cazul acestei
boli este inlocuirea hormonului masculin, a
testosteronului. Acesta duce la cresterea
pilozitatii pe corp, a masei musculare, a
increderii, ajuta in prevenirea ginecomastitei
si osteoporozei.
15. Ca efecte negative testosteronul poate
intensifica acneea, dezvolta anumite tulburari
de comportament si accentua prea rapid
dezvoltarea sexualitatii. Medicii recomanda
injectarea unei forme sintetice de testosteron
numita Depo-testosteron. In cazuri de
ginecomastie grava se poate recurge la
operatia de mastectomie ce consta in
indepartarea sanului. Acest procedeu insa nu
rezolva si problema infertilitatii.