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In 1976, Schaumann and Alter published the book Dermatoglyphics in Medical Disorders, which summarizes the findings of dermatoglyphic patterns under disease conditions. In 1982, Seltzer, et al., conducted a study on patients with breast cancer, and concluded that the presence of six or more whorls on a woman's fingertips indicated her being at ...
extremely rare, only 10 families worldwide are known to be affected with this disorder. Absence of fingerprints-congenital milia syndrome , also known simply as Baird syndrome is an extremely rare autosomal dominant genetic disorder which is characterized by a lack of fingerprints and the appearance of blisters and facial milia soon after birth ...
List of cutaneous conditions; References External links. This page was last edited on 23 May 2024, at 04:58 (UTC). Text is available under the Creative Commons ...
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. Five extended families worldwide are known to be affected by this condition.
Tel Hashomer camptodactyly syndrome is a rare genetic disorder which is characterized by camptodactyly,( a condition where one or more fingers or toes are permanently bent), facial dysmorphisms, and fingerprint, skeletal and muscular abnormalities. [2] [3] This disorder is thought to be inherited in an autosomal recessive fashion. [4]
Dermatopathia pigmentosa reticularis (DPR) is a rare, autosomal dominant [2] congenital disorder that is a form of ectodermal dysplasia.Dermatopathia pigmentosa reticularis is composed of the triad of generalized reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy. [3]
Stratton parker syndrome is a rare disorder characterized by short stature, wormian bones (extra cranial bones), and dextrocardia (displaced heart). [1] Other symptoms include dermatoglyphics, tooth deformities or missing teeth, abnormal kidney development, shortened limbs, intellectual disability, undescended testes or cryptorchidism, and anal atresia. [1]
Harold Cummins M.D. (May 28, 1893 – May 12, 1976) [1] [2] [3] was an anatomist and dermatoglyphics specialist. He is considered to be the founder of dermatoglyphics. He is considered to be the founder of dermatoglyphics.