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Research 181–210 of 1000+
- Muscle pain in a woman with congenital adrenal hyperplasia due to 21-hydroxylase deficiency resolved with testosterone therapy. A case report with 10 years of follow-up
- Clinical and trichoscopic features of early congenital syphilis: a single-center cross-sectional study
- Congenital cataract and slowly progressing facial skin lesions in a 5‐year‐old boy
- Congenital goiter in sibling goat kids
- Incidence of Congenital Goitre in Goats, in and Around Hyderabad, India
- Delayed Diagnosis of Congenital Adrenal Hyperplasia Due to 3β-Hydroxysteroid Dehydrogenase Type 2 Deficiency
- A Case of Basal Cell Carcinoma Arising in Congenital Triangular Alopecia
- Neuroimaging Findings in Congenital Biotinidase Deficiency: A Case Report
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- A Case of Congenital Alopecia Areata Successfully Diagnosed by Integrating Clinical, Trichoscopic, and Scalp Biopsy Findings
- Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
- Multiple congenital smooth muscle hamartoma: A case report
- Line-Field Optical Coherence Tomography: Usefulness in the Non-Invasive Differential Diagnosis of Congenital Alopecia of Infancy
- A Rare Case Report of Congenital Adrenal Hyperplasia: 46XX at Tertiary Care Centre, Visnagar, North Gujarat.
- Congenital Triangular Alopecia: A Case of Effective Response with 5% Topical Minoxidil in a Male Adolescent
- Rare Association of Congenital Triangular Alopecia with Vitiligo
- Congenital erythropoietic porphyria five years observation with standard treatment: a case report
- Syndromic or non-syndromic congenital ichthyosis? A case report of two brothers with ichthyosis but microphthalmia and blindness in only one brother
- Congenital Atrichia: A Case Report
- Isotretinoin-unresponsive acne as a sign of a congenital disorder: a case of 21-hydroxylase deficiency
- Congenital alopecia areata: a systematic review
- Approaching fertility in congenital adrenal hyperplasia: exploring P30L mutation-induced 21-hydroxylase deficiency with a presentation between non-classical and simple virilizing phenotypes. A case report
- PA31 Congenital alopecia areata: a systematic review
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Congenital Adrenal Hyperplasia
- T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy
- Genes of Congenital Dermatologic Disorders in Dogs—A Review
- Congenital Trichomegaly of the Eyelashes