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Newborns with harlequin-type ichthyosis present with thick, fissured armor-plate hyperkeratosis. [11] Sufferers feature severe cranial and facial deformities. The ears may be very poorly developed or absent, as may the nose. The eyelids may be everted , which leaves the eyes and the area around them very susceptible to infection. [12]
Rh disease (also known as rhesus isoimmunization, Rh (D) disease, or rhesus incompatibility, and blue baby disease) is a type of hemolytic disease of the fetus and newborn (HDFN). HDFN due to anti-D antibodies is the proper and currently used name for this disease as the Rh blood group system actually has more than 50 antigens and not only the ...
Susan has navy blue (later cyan blue) eyes, wears black skirt, knee-high socks, a pair of Mary Janes, and a light blue t-shirt depicting a blue star. She has straight red hair, is held with a yellow star-shaped clip, and wears square-shaped glasses. Susan tends to be more irritable and harsh than Mary is, which often leads to her downfall.
Waardenburg syndrome is a group of rare genetic conditions characterised by at least some degree of congenital hearing loss and pigmentation deficiencies, which can include bright blue eyes (or one blue eye and one brown eye), a white forelock or patches of light skin.
A California baby, born prematurely at 26 weeks, is a true rarity. This is 10-week-old Silas Phillips. He was born via cesarean section , completely enclosed in his amniotic sac, something known ...
The blue baby syndrome or cyanosis occurs when absolute amount of deoxygenated hemoglobin > 3g/dL which is typically reflected with an O 2 saturation of < 85 %. [ 1 ] Both of these conditions cause cyanosis , or a bluish discoloration of skin or mucous membranes. [ 4 ]
Individuals with Ectodermal Dysplasia (ED) commonly experience sparse or absent hair, a condition known as hypotrichosis. Scalp hair is typically fine, brittle, and may lack pigmentation, appearing light or wispy. Eyebrows and eyelashes may also be sparse or absent, contributing to the distinct facial appearance seen in ED.
Mongolian spot is a congenital developmental condition—that is, one existing from birth—exclusively involving the skin.The blue colour is caused by melanocytes, melanin-containing cells, that are usually located in the surface of the skin (the epidermis), but are in the deeper region (the dermis) in the location of the spot. [6]