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Turnerov syndróm
Č. záznamu d014424 Dátum 06.06.2025 Typ M Tematický termín Turnerov syndróm Iný termín Angličtina (Pseudonym) Bonnevie-Ullrich Syndrome
Angličtina (Pseudonym) Gonadal Dysgenesis, 45,X
Angličtina (Pseudonym) Gonadal Dysgenesis, XO
Slovenčina (Pseudonym) dysgenéza gonadálna, 45,X
Slovenčina (Pseudonym) dysgenéza gonadálna, XO
Slovenčina (Pseudonym) Bonnevieovej-Ullrichov syndróm
Slovenčina (Pseudonym) Bonnevie-Ullrich syndróm
Slovenčina (Pseudonym) stav popísaný Bonnevieovou-Ullrichom
Slovenčina (Pseudonym) Ullrichov-Turnerov syndróm
Slovenčina (Pseudonym) monozómia X
Pozri tiež (Novšie záhlavie) Noonanovej syndróm
(Skutočné meno) Noonanovej syndróm
MDT C12.050.351.875.253.309.872C12.050.351.875.253.795.750C12.200.706.316.309.872C12.200.706.316.795.750C12.800.316.309.872C12.800.316.795.750C14.240.400.980C14.280.400.980C16.131.240.400.970C16.131.260.830.835.750C16.131.939.316.309.872C16.131.939.316.795.750C16.320.180.830.835.750C19.391.119.309.872C19.391.119.795.750 Poznámka A syndrome of defective gonadal development in phenotypic females associated with the karyotype 45,X (or 45,XO). Patients generally are of short stature with undifferentiated GONADS (streak gonads), SEXUAL INFANTILISM, HYPOGONADISM, webbing of the neck, cubitus valgus, elevated GONADOTROPINS, decreased ESTRADIOL level in blood, and CONGENITAL HEART DEFECTS. NOONAN SYNDROME (also called Pseudo-Turner Syndrome and Male Turner Syndrome) resembles this disorder; however, it occurs in males and females with a normal karyotype and is inherited as an autosomal dominant. 
predmetové heslo
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