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Case Reports
. 2025 Jan 20:15:1491870.
doi: 10.3389/fgene.2024.1491870. eCollection 2024.

Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report

Affiliations
Case Reports

Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report

Mingyue Zhuang et al. Front Genet. .

Abstract

Hypotrichosis simplex of the scalp (HSS) is a clinically rare monogenic autosomal dominant disorder associated with variants in the gene CDSN, which encodes the desmosome protein corneodesmosin. Although studies have reported that some medications can improve the symptoms of hair loss in HSS, there is still a lack of definitive and effective treatments for this disease. We report a familial case of HSS in an 8-year-old male child diagnosed with HSS caused by a mutation in CDSN, who was treated with botanical extracts in combination with minoxidil, which resulted in significant hair growth after two treatments. This is the first study describing the improvement of clinical symptoms of HSS with oral botanical extracts. This suggests that botanical extracts in combination with minoxidil may be a therapeutic approach for HSS in the clinic.

Keywords: botanical extracts; family genealogy; genetic mutation; hair disease; hypotrichosis simplex of the scalp.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

FIGURE 1
FIGURE 1
Comparison of hair before and after treatment. (A–C) Before treatment, the patient’s hair was thinning. (D–F) 6 months after treatment, a notable improvement in the patient’s hair condition was observed.
FIGURE 2
FIGURE 2
Sanger sequencing results of the CDSN gene in the patient and his relatives. The mutation c.701C > A is indicated by an arrow. (A) patient has heterozygous mutation in CDSN gene c.701C > A (p.Ser234*). (B) His father’s CDSN gene is wild-type. (C–D) H is mother and maternal grandfather carried the same heterozygous mutation in CDSN gene c.701C > A (p.Ser234*).

References

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