Obsterics & Gynecology
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Tarmoq:📈 Telegram kanali Obsterics & Gynecology analitikasi
Obsterics & Gynecology (@obs_gynee) Ingliz til segmentidagi kanali faol ishtirokchi. Hozirda hamjamiyat 25 478 obunachidan iborat bo'lib, Tibbiyot toifasida 849-o'rinni va Hindiston mintaqasida 15 819-o'rinni egallagan.
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невідомо sanasidan buyon loyiha tez o‘sib, 25 478 obunachiga ega bo‘ldi.
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- Jalb etish (ER): Auditoriya o‘rtacha 10.20% darajada jalb etiladi. Nashrdan keyingi dastlabki 24 soatda kontent odatda umumiy obunachilar sonining 2.43% ini tashkil etuvchi reaksiyalarni to‘playdi.
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Yuqori yangilanish chastotasi (oxirgi ma’lumot 28 Oktabr, 2026 da olingan) sababli kanal doimo dolzarb va katta qamrovli bo‘lib qoladi. Analitika auditoriya kontent bilan faol hamkorlik qilishini, uni Tibbiyot toifasidagi muhim ta’sir nuqtasiga aylantirishini ko‘rsatadi.
25 478
Obunachilar
+1724 soatlar
+1377 kun
+49830 kun
Postlar arxiv
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Obsterics & Gynecology:
Ans is c
Correct Answer - A Obliteration of the umbilical vein
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Correct Answer - D
Correct Ans: D. Hegar's sign
At 6 to 8 weeks menstrual age, the firm cervix contrasts with the now
softer fundus and the compressible interposed softened isthmus
—Hegar sign
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In early pregnancy clinical signs of
feeling the cervix and the body of bulky
uterus separated because of softened isthmus at 6 - 8 weeks of gestation :
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Correct Answer - A
Ans. A. 21 alpha-hydroxylase
The condition described above represents the Congenital adrenal
hyperplasia.
"More than 90% of CAH cases are caused by 21-hydroxylase
deficiency"
Congenital adrenal hyperplasia:
It is due to an inborn error of adrenal steroid metabolism, commonly
due to 21-hydroxylase (95%) and rarely due to 11-hydroxylase or 3β
hydroxysteroid dehydrogenase deficiency.
Clinical presentation
An ambiguity of sex at birth
Hirsutism and amenorrhea may be the presenting features around
puberty in a milder form.
The karyotype is 46, XX.
Ref. Dutta Gynaecology ed. 6th page no. 440
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25 478
13 yr old child visit gynaecology OPD
with a complaint of not attaining
menarche with karyotype 46XX. On examination, clitoromegaly is seen. Which enzyme is most likely to be deficient in the above condition?
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25 478
Correct Answer - A
Ans. A. 21 alpha-hydroxylase
The condition described above represents the Congenital adrenal
hyperplasia.
"More than 90% of CAH cases are caused by 21-hydroxylase
deficiency"
Congenital adrenal hyperplasia:
It is due to an inborn error of adrenal steroid metabolism, commonly
due to 21-hydroxylase (95%) and rarely due to 11-hydroxylase or 3β
hydroxysteroid dehydrogenase deficiency.
Clinical presentation
An ambiguity of sex at birth
Hirsutism and amenorrhea may be the presenting features around
puberty in a milder form.
The karyotype is 46, XX.
Ref. Dutta Gynaecology ed. 6th page no. 440
25 478
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25 478
13 yr old child visit gynaecology OPD
with a complaint of not attaining
menarche with karyotype 46XX. On examination, clitoromegaly is seen. Which enzyme is most likely to be deficient in the above condition?
25 478
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