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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.
adermatoglyphia with neo-natal blisters and facial milia: Complications: Usually none (health-wise), however; hypohidrosis may lead to heat exhaustion or even a heat stroke, and the absence of fingerprints may complicate the use of systems that require fingerprint-identification: Usual onset: Birth: Duration: Life-long: Types: Adermatoglyphia ...
Dermatoglyphics, when correlated with genetic abnormalities, aids in the diagnosis of congenital malformations at birth or soon after.. Klinefelter syndrome: excess of arches on digit 1, more frequent ulnar loops on digit 2, overall fewer whorls, lower ridge counts for loops and whorls as compared with controls, and significant reduction of the total finger ridge count.
Adermatoglyphia; Adiposis dolorosa; Adiposogenital dystrophy; Adipsia; Adrenoleukodystrophy; Adult polyglucosan body disease; Adult-onset Still's disease; Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome; Aggressive fibromatosis; AIDS dysmorphic syndrome; Albright's hereditary osteodystrophy; Aldolase A deficiency ...
Most cases are caused by mutations in the EDA gene, which are inherited in an X-linked recessive pattern, called x-linked hypohidrotic ectodermal dysplasia (XLHED). A condition is considered X-linked if the mutated gene that causes the disorder is located on the X chromosome, one of the two sex chromosomes.
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]
Autosomal dominant Charcot–Marie–Tooth disease type 2 with giant axons; Autosomal dominant GTP cyclohydrolase I deficiency; Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome; Autosomal dominant nocturnal frontal lobe epilepsy; Autosomal dominant partial epilepsy with auditory features
C. Calcifying epithelioma of Malherbe; Capillary hemangioma; Cephalic brain-like heterotopia; Cervical accessory tragus; Congenital absence of skin; Congenital auricular fistula