Rud syndrome

Rud syn·drome

(rūd),
ichthyosiform erythroderma associated with acanthosis nigricans, dwarfism, hypogonadism, and epilepsy; mostly sporadic, but may be an X-linked recessive trait.

Rud syn·drome

(rūd sin'drōm)
Ichthyosiform erythroderma associated with acanthosis nigricans, dwarfism, hypogonadism, and epilepsy; mostly sporadic, but may be an X-linked recessive trait.

Rud,

Einar, Danish physician, 1892-1933.
Rud syndrome - ichthyosiform erythroderma associated with acanthosis nigricans, dwarfism, hypogonadism, and epilepsy.
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References in periodicals archive ?
Clinical findings led to a differential diagnosis of Sjogren-Larsson syndrome, Refsum disease, Rud syndrome, and Chanarin-Dorfman syndrome, and so genetic testing was performed.