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Research 271–300 of 1000+
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Congenital Lipedematous Alopecia in a 6-Year-Old Asian Boy
- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review
- Challenges in the Diagnosis of Simple-Virilizing Congenital Adrenal Hyperplasia: A Case Report
- Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year
- Giant Congenital Blue Nevus Presenting as Cutis Verticis Gyrata: A Case Report and Review of the Literature
- Nonclassical Congenital Adrenal Hyperplasia and Pregnancy
- Familial congenital generalized hypertrichosis
- Giant congenital cerebriform pigmented nevus of scalp: case report
- Hereditary, Congenital, and Acquired Alopecias
- (26) Acne due to congenital adrenal hyperplasia
- Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency epidemiology, etiopathogenesis, clinical presentation, treatment – a systematic review
- Congenital Hypotrichosis with Hair and Dental Ectodermal Features Responsive to Sublingual Minoxidil
- 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
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- 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