Review Note

Last Update: 08/13/2023 06:55 PM

Current Deck: L1 Pediartic Patholgy 1

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{{c2::Turner}} syndrome is most commonly characterized by a {{c1::45}},{{c1::XO}} karyotype

Extra

- most cases are caused by sperm lacking X chromosome due to meiotic nondisjunction

- other causes include:

short arm deletion (46 X,del(Xp))

isochromosome 46 X,i(Xq)

somatic mosaicism (45XO,46XX); most common diagnosed mosaicism affecting sex chromosomes, these patients typically have a milder form of Turner syndrome or can be asymptomatic

Lecture Notes

Missed Questions

Pathoma

Boards and Beyond

First Aid

Sketchy

Pixorize

Physeo

OME

Additional Resources

Tags:

#AK_Step1_v10::#AMBOSS::Reproductive #AK_Step1_v10::#B&B::10_Genetics::02_Disorders::06_Turner_&_Klinefelter_Syndromes #AK_Step1_v10::#FirstAid::15_Repro::04_Pathology::01_Sex_Chromosome_Disorders::Turner_Syndrome

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