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Specialty. Medical genetics. Distal 18q- is a genetic condition caused by a deletion of genetic material within one of the two copies of chromosome 18. [1] The deletion involves the distal section of 18q and typically extends to the tip of the long arm of chromosome 18. [2]
Structures opening in the vulval vestibule are the urethra (urinary meatus), vagina, Bartholin's glands, and Skene's glands. [1]The external urethral orifice is placed about 25–30 millimetres (1–1.2 in) [2] behind the clitoris and immediately in front of that of the vagina; it usually assumes the form of a short, sagittal cleft with slightly raised margins.
Individuals with ring 18 have one of their two copies of chromosome 18 that has formed the shape of a ring. The ring is formed when the caps on both the long arm (q) and the short arm (p) of one copy of chromosome 18 are lost and the new ends re-join to form the ring. Because the ring involves deletions of both the long arm (18q-) and the short ...
In amniotes, the clitoris (/ ˈklɪtərɪs / ⓘ KLIT-ər-iss or / klɪˈtɔːrɪs / ⓘ klih-TOR-iss; pl.: clitorises or clitorides) is a female sex organ. [ 1 ] In humans, it is the vulva 's most erogenous area and generally the primary anatomical source of female sexual pleasure. [ 2 ] The clitoris is a complex structure, and its size and ...
1 per 5,000 births [3] Trisomy 18, also known as Edwards syndrome, is a genetic disorder caused by the presence of a third copy of all or part of chromosome 18. [3] Many parts of the body are affected. [3] Babies are often born small and have heart defects. [3] Other features include a small head, small jaw, clenched fists with overlapping ...
Anatomical terminology. [edit on Wikidata] In mammals, the vulva (pl.: vulvas or vulvae) comprises mostly external, visible structures of the female genitalia leading away from the interior parts of the female reproductive tract, starting at the vaginal opening. For humans, it includes the mons pubis, labia majora, labia minora, clitoris ...
NC_000018 (FASTA) GenBank. CM000680 (FASTA) Chromosome 18 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 18 spans about 80 million base pairs (the building material of DNA) and represents about 2.5 percent of the total DNA in cells.
Sex differences. v. t. e. Disorders of sex development (DSDs), also known as differences in sex development or variations in sex characteristics (VSC), [ 2 ][ 3 ] are congenital conditions affecting the reproductive system, in which development of chromosomal, gonadal, or anatomical sex is atypical. [ 4 ]