Hypotrichosis | List of Frontiers open access articles

Original Research

Published on 06 Jan 2023

A novel homozygous mutation in LSS gene possibly causes hypotrichosis simplex in two siblings of a Tibetan family from the western Sichuan province of China

in Clinical and Translational Physiology

Bei Zhao
Yisi Tang
Wenjing Chen
Huiying Wan
Jiyun Yang
Xuejun Chen

Frontiers in Physiology

doi 10.3389/fphys.2022.992190

4,480 views
6 citations

Case Report

Published on 29 Apr 2025

Congenital hypotrichosis caused by compound heterozygous variants in the LSS gene in a Chinese patient with strabismus: case report

in Genetics of Common and Rare Diseases

Linlin Bao
Qian Li
Zhicao Yue
Fang Yang

Frontiers in Pediatrics

doi 10.3389/fped.2025.1512646

1,954 views

Case Report

Published on 17 Aug 2022

Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles

in Genetics of Common and Rare Diseases

Khalid Al Hawsawi
Mazin Al Jabri
Mazen S. Dajam
Bashaer Almahdi
Waseem K. Alhawsawi
Safdar Abbas
Abeer Al Tuwaijri
Muhammad Umair
Majid Alfadhel
Sultan Al-Khenaizan

Frontiers in Genetics

doi 10.3389/fgene.2022.994509

2,397 views
1 citation

Case Report

Published on 20 Jan 2026

Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14

in Dermatology

Yonglong Xu
Dingquan Yang
Ying Xie
Qingwu Liu
Shuying Lv
Meijiao Du
Lei Wang

Frontiers in Medicine

doi 10.3389/fmed.2026.1669753

388 views

Case Report

Published on 20 Jan 2025

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

in Genetics of Common and Rare Diseases

Mingyue Zhuang
Yonglong Xu
Shiyi Zhong
Ziyuan Tian
Qingwu Liu
Dingquan Yang

Frontiers in Genetics

doi 10.3389/fgene.2024.1491870

4,343 views

Original Research

Published on 11 Aug 2021

Correction of Vertebral Bone Development in Ectodysplasin A1-Deficient Mice by Prenatal Treatment With a Replacement Protein

in Genetics of Common and Rare Diseases

Clara-Sophie Kossel
Mandy Wahlbuhl
Sonia Schuepbach-Mallepell
Jung Park
Christine Kowalczyk-Quintas
Michaela Seeling
Klaus von der Mark
Pascal Schneider
Holm Schneider

Frontiers in Genetics

doi 10.3389/fgene.2021.709736

3,174 views
4 citations

Original Research

Published on 03 Aug 2021

Whole Exome Sequencing Confirms Molecular Diagnostics of Three Pakhtun Families With Autosomal Recessive Epidermolysis Bullosa

in Genetics of Common and Rare Diseases

Fozia Fozia
Rubina Nazli
Nousheen Bibi
Sher Alam Khan
Noor Muhammad
Nafila Shakeeb
Saadullah Khan
Musharraf Jelani
Naveed Wasif

Frontiers in Pediatrics

doi 10.3389/fped.2021.727288

4,685 views
4 citations

Original Research

Published on 15 Jul 2024

Exome sequencing confirms the clinical diagnosis of both joubert syndrome and klinefelter syndrome with keratoconus in a han Chinese family

in Genetics of Common and Rare Diseases

Xinhe Fang
Meijiao Ma
Weining Rong
Yuan-Yuan Lian
Xueli Wu
Yongying Gao
Hui-Ping Li
Xunlun Sheng

Frontiers in Genetics

doi 10.3389/fgene.2024.1417584

5,429 views

Articles

A novel homozygous mutation in LSS gene possibly causes hypotrichosis simplex in two siblings of a Tibetan family from the western Sichuan province of China

Congenital hypotrichosis caused by compound heterozygous variants in the LSS gene in a Chinese patient with strabismus: case report

Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles

Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14

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

Correction of Vertebral Bone Development in Ectodysplasin A1-Deficient Mice by Prenatal Treatment With a Replacement Protein

Whole Exome Sequencing Confirms Molecular Diagnostics of Three Pakhtun Families With Autosomal Recessive Epidermolysis Bullosa

Exome sequencing confirms the clinical diagnosis of both joubert syndrome and klinefelter syndrome with keratoconus in a han Chinese family