Search
for
Did you mean Congenital Alopecia?
Sort by
Research 30 of 1000+
- Long-Term Follow-up and Unusual Findings After Microvascular Transfer of Hair-Bearing Skin for Pubic Hair Restoration
- Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
- “Case Report : Early Congenital Syphilis”
- The eye and the skin in endocrine metabolic diseases
- Nevus Sebaceus With Novel HRAS Sequence Variant Mutation Misdiagnosed as Alopecia Areata
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- Acquired Acrodermatitis Enteropathica in an Infant
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- An Update of Congenital Adrenal Hyperplasia
- Congenital adrenal hyperplasia
- Congenital atrichia and hypotrichosis
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Hair Loss in Children
- Alternative uses of dermoscopy in daily clinical practice: An update
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Acquired 11β-hydroxylase Deficiency by Inhaled Etomidate and its Analogues: A Mimic of Congenital Adrenal Hyperplasia
- Congenital atrichia with papular lesions
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Síndrome postfinasterida y disfunción eréctil. Caso clínico y revisión de la literatura
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Polarized microscopy in genetic hair disorders: case series
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Acne Syndromes and Mosaicism
- Role of Trichoscopy in diagnosing Genotrichosis—A Report of Two Cases
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Clinical and trichoscopic features of early congenital syphilis: a single-center cross-sectional study