Search results
Results from the WOW.Com Content Network
Female rats wiggle their ears when they are in heat, to excite male rats and encourage them to mate. [4] Ear wiggling was a shtick in Hal Roach comedies such as Laurel and Hardy and Our Gang. To achieve this effect, performers such as Stan Laurel would have their ears pulled by threads which would not be visible in the film. [5]
TBS patients may have the following symptoms: [3] Abnormalities of the external ears (unusually large or small, unusually shaped, sometimes with sensorineural hearing loss or deafness due to lesions or dysfunctions of part of the internal ear or its nerve tracts and centers or conductive hearing loss from the external or middle ear), dysplastic ears, lop ear (over-folded ear helix ...
Seckel syndrome, or microcephalic primordial dwarfism (also known as bird-headed dwarfism, Harper's syndrome, Virchow–Seckel dwarfism and bird-headed dwarf of Seckel [1]) is an extremely rare congenital nanosomic disorder.
Analysis of the pedigree using the principles of Mendelian inheritance can determine whether a trait has a dominant or recessive pattern of inheritance. Pedigrees are often constructed after a family member afflicted with a genetic disorder has been identified. This individual, known as the proband, is indicated on the pedigree by an arrow. [5]
The muscles connected to the ears of a human do not develop enough to have the same mobility allowed to monkeys. Arrows show the vestigial structure called Darwin's tubercle . In the context of human evolution , vestigiality involves those traits occurring in humans that have lost all or most of their original function through evolution .
Later research adopted more advanced techniques and more sophisticated statistical analysis. [6] Hairy ears are an example of a gene once thought to be Y-linked in humans; however, that hypothesis was discredited. [5] Due to advancements in DNA sequencing, Y linkage is getting easier to determine and prove.
The varying clinical expression of the disease between different families suggests that multiple loci may be involved. In 1992, using genetic linkage studies, the BOR gene was identified on chromosome 8, [10] Subsequently, another locus on human chromosome 14 was identified, and several mutations were reported in genes EYA1, SIX1, [11] and SIX5.
Microtia is a congenital deformity where the auricle (external ear) is underdeveloped. A completely undeveloped auricle is referred to as anotia.Because microtia and anotia have the same origin, it can be referred to as microtia-anotia. [1]