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The gluteal sulcus (also known as the gluteal fold, tuck, fold of the buttock, horizontal gluteal crease, or gluteal furrow) is an area of the body of humans and anthropoid apes, described by a horizontal crease formed by the inferior aspect of the buttocks and the posterior upper thigh. [1]
Michelin tire baby syndrome (also known as Kunze–Riehm syndrome [1] and "folded skin with scarring" [2]: 625 ), is a condition occurring in babies that is characterized by multiple, symmetric, circular skin creases, or bands, on the forearms, lower legs, and often the neck that are present at birth. The creases disappear later in life.
Atypical dimples can also be deep, positioned above the gluteal crease, located outside the midline, or occur as multiple dimples. [8] Sacral dimples are often spotted in post-natal checks by pediatricians, [3] [5] who can check: whether the floor of the dimple is covered with skin; whether there is a tuft of hair in the dimple;
Abnormal findings in physical assessments usually result in employing other diagnostic tests to ascertain the diagnosis. Genetic testing is the most specific diagnostic test for harlequin ichthyosis. This test reveals a loss of function mutation on the ABCA12 gene. [ 18 ]
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A wide variety of abnormalities of the hands and feet, including the nails and the creases of the hand, have been described and differentiated. [4] Many of these abnormalities do not have an impact on function but may be useful in diagnosing genetic syndromes; for example, the single transverse palmar crease is commonly associated with Down ...
Sclerema neonatorum is a rare and severe skin condition that is characterized by diffuse hardening of the subcutaneous tissue with minimal inflammation. [1] [2] Sclerema neonatorum is categorized as a kind of panniculitis that appears as subcutaneous adipose tissue and skin hardening. The hardened skin and subcutaneous fat stick to the ...
Wrinkly skin syndrome (WSS) is a rare genetic condition characterized by sagging, wrinkled skin, low skin elasticity, and delayed fontanelle (soft spot) closure, along with a range of other symptoms. [1] The disorder exhibits an autosomal recessive inheritance pattern with mutations in the ATP6V0A2 gene, leading to abnormal glycosylation events ...
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