Cutaneous congenital anomalies

benign, flat, congenital birthmark, prevalent among East, South, Southeast, North and Central Asian peoples, Indigenous Oceanians, and Amerindians

tissue disease

additional nipple occurring in mammals

abnormal, epithelial-lined connection between an artery and vein that is present at the time of birth

human anatomy

Adermatoglyphia is an extremely rare genetic disorder that prevents the development of fingerprints. Five extended families worldwide are known to be affected by this condition.

congenital benign cyst arising from the remnants of the thyroglossal duct

human disease

tumor derived from branchial epithelium or branchial rests

medical condition

Pilomatricoma is a benign skin tumor derived from the hair matrix. These neoplasms are relatively uncommon and typically occur on the scalp, face, and upper extremities. Clinically, pilomatricomas present as a subcutaneous nodule or cyst with unremarkable overlying epidermis that can range in size from 0.5 to 3.0 cm, but the largest reported case was 24 cm.

clinical sign of congenital syphilis

thumb|Fissures, or rhagades (photo from "An American text-book of the diseases of children" (1895)) Rhagades' are fissures, cracks, or linear scars in the skin, especially at the angles of the mouth and nose. They tend to form at areas of motion. They can be a result from bacterial infection of skin lesions. They are one of the late-stage manifestations of congenital syphilis; others are saber shins, Hutchinson teeth, saddle nose, and Clutton's joints (usually knee synovitis).

macular lesion on the side of the face

Dyschromia refers to an alteration of the color of the skin or nails.

most common variant of hemangioma, dull red, firm, dome-shaped hemangioma, usually located on the head and neck, which grows rapidly caused by proliferation of immature capillary vessels

cutaneous condition characterized by multiple congenital abnormalities. ("PHACES"=Posterior fossa malformations–hemangiomas–arterial anomalies–cardiac defects–eye abnormalities–sternal cleft and supraumbilical raphe syndrome)

Human disease

physical human trait

acrofacial dysostosis characterized by underdeveloped cheek bones, very small lower jaw, cleft palate, defects in the middle ear, absent eyelashes, and a notch in the lower eyelids called a coloboma, in children