Partial androgen insensitivity syndrome
Partial androgen insensitivity syndrome (PAIS) is a condition that results in the partial inability of the cell to respond to androgens. It is an X linked recessive condition. The partial unresponsiveness of the cell to the presence of androgenic hormones impairs the masculinization of male genitalia in the developing fetus, as well as the development of male secondary sexual characteristics at puberty, but does not significantly impair female genital or sexual development. As such, the insensitivity to androgens is clinically significant only when it occurs in individuals with a Y chromosome (or more specifically, an SRY gene). Clinical features include ambiguous genitalia at birth and primary amenhorrhoea with clitoromegaly with inguinal masses. Mullerian structures are not present in th
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Androgen insensitivity syndrome1,2-dimethoxyethaanAndrostanoloneAnick SoniComplete androgen insensitivity syndromeDisorders of sex developmentEliana RubashkynGilbert-Dreyfus syndromeIncomplete testicular feminizationIntersex and LGBTIntersex people in historyList of diseases (R)List of syndromesLub's syndromeMild androgen insensitivity syndromePAISPartial Androgen Insensitivity SyndromeQuigley scaleReifensteinReifenstein's syndromeReifenstein SyndromeReifenstein syndromeRosewater syndromeSean Saifa WallSmall LukTony Briffa (politician)
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Partial androgen insensitivity syndrome
Partial androgen insensitivity syndrome (PAIS) is a condition that results in the partial inability of the cell to respond to androgens. It is an X linked recessive condition. The partial unresponsiveness of the cell to the presence of androgenic hormones impairs the masculinization of male genitalia in the developing fetus, as well as the development of male secondary sexual characteristics at puberty, but does not significantly impair female genital or sexual development. As such, the insensitivity to androgens is clinically significant only when it occurs in individuals with a Y chromosome (or more specifically, an SRY gene). Clinical features include ambiguous genitalia at birth and primary amenhorrhoea with clitoromegaly with inguinal masses. Mullerian structures are not present in th
has abstract
El síndrome de insensibilidad ...... recen de una necesidad médica.
@es
Partial androgen insensitivity ...... to engage in penetrative sex.
@en
Синдро́м Рейфенште́йна (синдро ...... ую терапию или вагинопластику.
@ru
متلازمة عدم الحساسية الجزئية ل ...... ة الجنس ولديها 46 XY كروموسوم.
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DiseasesDB
eMedicine subject
ped
@en
eMedicine topic
2222
@en
geneReviewsId
geneReviewsName
Androgen Insensitivity Syndrome
@en
ICD10
ICD9
MeSH ID
OMIM id
ORPHA
Wikipage page ID
page length (characters) of wiki page
Wikipage revision ID
1,024,863,895
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caption
AIS results when the function ...... f androgens in the human body.
@en
colwidth
DiseasesDB
eMedicineSubj
ped
@en
eMedicineTopic
GeneReviewsName
Androgen Insensitivity Syndrome
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GeneReviewsNBK
NBK1429
@en
ICD
MeshID
D013734
@en
OMIM
Orphanet
SNOMED CT
122,811,000,119,101
synonyms
Partial androgen resistance syndrome; Reifenstein syndrome
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wikiPageUsesTemplate
hypernym
comment
El síndrome de insensibilidad ...... ambiguos en el nacimiento y pr
@es
Partial androgen insensitivity ...... ructures are not present in th
@en
Синдро́м Рейфенште́йна (синдро ...... нного типа при рождении и перв
@ru
متلازمة عدم الحساسية الجزئية ل ...... و بشكل أكثر تحديدًا، جين SRY).
@ar
label
Partial androgen insensitivity syndrome
@en
Síndrome de insensibilidad parcial a los andrógenos
@es
Синдром Рейфенштейна
@ru
متلازمة عدم الحساسية الجزئية للأندروجين
@ar