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Two new enzymes, PAD-R11 and PAD-R4, were cloned and showed activity, with PAD-R11 resembling epidermal enzymes.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Retinoids or their analogs could treat skin pigmentation disorders like melasma and vitiligo.

A girl had rickets due to a gene mutation affecting vitamin D response.

Efficient enzyme function relies on specific residue interactions and structural coordination.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

This enzyme helps metabolize fatty acids and isoleucine, and could be key in treating neurological diseases and certain cancers.

A girl with type 1 diabetes developed a serious eye condition very early, suggesting the need for earlier eye checks and that early treatment can work well.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

The enzyme 5α-reductase is important for proper blood vessel development during the fertility-related transformation of the uterus lining.

RXRa is crucial for Th2 immune cell development and may link nutrition to immune health.

Retinoids can help treat skin pigmentation disorders by affecting melanin production.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

Measuring 24-OHase induction helps identify defects in vitamin D processing and predict treatment response.

The enzyme 5α-reductase type 1 is important for blood vessel development and fertility in the uterus.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

Increased 11β-HSD1 activity in skin may contribute to aging and could be targeted to reduce aging effects.

The P133R mutation in AKR1D1 enzyme causes harmful bile acid buildup, explaining related health issues.

VDDR I and II are genetic disorders affecting vitamin D use, causing rickets, with VDDR I treatable by vitamin D supplements and VDDR II needing high doses and calcium.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

The document's conclusion cannot be provided because the document is not available or cannot be read.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.

DPR can show different hair characteristics, as seen in two brothers with normal hair.

Four patients with a type of rickets and hair loss had different mutations in their vitamin D receptor gene, causing it to not work properly.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

The structure of SRD5A reveals how it reduces steroids, aiding drug design for related health conditions.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.