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  2. Adermatoglyphia - Wikipedia

    en.wikipedia.org/wiki/Adermatoglyphia

    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.

  3. Absence of fingerprints-congenital milia syndrome - Wikipedia

    en.wikipedia.org/wiki/Absence_of_fingerprints...

    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 ...

  4. Dermatoglyphics - Wikipedia

    en.wikipedia.org/wiki/Dermatoglyphics

    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.

  5. Hypohidrotic ectodermal dysplasia - Wikipedia

    en.wikipedia.org/wiki/Hypohidrotic_ectodermal...

    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.

  6. Naegeli–Franceschetti–Jadassohn syndrome - Wikipedia

    en.wikipedia.org/wiki/Naegeli–Franceschetti...

    Naegeli–Franceschetti–Jadassohn syndrome (NFJS), also known as chromatophore nevus of Naegeli and Naegeli syndrome, [1] [2] is a rare autosomal dominant [3] form of ectodermal dysplasia, characterized by reticular skin pigmentation, diminished function of the sweat glands, the absence of teeth and hyperkeratosis of the palms and soles.

  7. Dermatopathia pigmentosa reticularis - Wikipedia

    en.wikipedia.org/wiki/Dermatopathia_pigmentosa...

    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]

  8. Collagen induction therapy - Wikipedia

    en.wikipedia.org/wiki/Collagen_induction_therapy

    Some studies have also shown that when combined with minoxidil treatment, microneedling is able to treat hair loss more effectively than minoxidil treatment alone. [2] Platelet-rich plasma (PRP) can be combined with collagen induction therapy treatment in a form of dermatologic autologous blood therapy.

  9. Acute generalized exanthematous pustulosis - Wikipedia

    en.wikipedia.org/wiki/Acute_generalized...

    The treatment of AGEP begins with the immediate cessation of the offending drug. For individuals developing AGEP while taking multiple drugs, non-essential drugs should be discontinued and essential drugs should be replaced by chemically unrelated drugs that are used as alternatives to the discontinued drug(s).