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A particular type of anatomically correct dolls are used in law enforcement and therapy. These dolls have detailed depictions of all the primary and secondary sexual characteristics of a human: "oral and anal openings, ears, tongues, nipples, and hands with individual fingers" for all and a "vagina, clitoris and breasts" for each of the female dolls and a "penis and testicles" for each of the ...
Low-set ears are defined as the outer ears being positioned two or more standard deviations lower than the population average. [1] Clinically, if the point at which the helix (curved upper part) of the outer ear meets the cranium is at or below the line connecting the inner canthi of eyes (the bicanthal plane), the ears are considered low set ...
Boy with otapostasis. Father and son with otapostasis. Protruding ear, otapostasis or bat ear is an abnormally prominent human ear. It may be unilateral or bilateral. The concha is large with poorly developed antihelix and scapha. It is the result of malformation of cartilage during primitive ear development in intrauterine life. [1]
Angelman syndrome; Other names: Angelman's syndrome [1] [2]: A five-year-old girl with Angelman syndrome. Features shown include telecanthus, bilateral epicanthic folds, small head, wide mouth, and an apparently happy demeanor; hands with tapered fingers, abnormal creases and broad thumbs.
In 1943 Konrad Lorenz noted that a newborn infant's rounded facial features might encourage guardians to show greater care for them, due to their perceived cuteness. He labeled this the Kewpie doll effect , because of their similarity to the eponymous doll.
Sometimes, Emina also takes commissions, specifically for pet dolls, and they are absolutely adorable!In an interview with Bored Panda, the artist shared about her creative process: "First, an ...
An image of an impassioned girl yelling into the ear of a guy who appears indifferent to what she's saying has captivated the internet. She's the "girl explaining" — and seemingly everyone finds ...
Saethre–Chotzen syndrome (SCS), also known as acrocephalosyndactyly type III, is a rare congenital disorder associated with craniosynostosis (premature closure of one or more of the sutures between the bones of the skull). This affects the shape of the head and face, resulting in a cone-shaped head and an asymmetrical face.