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Pigmentary changes and atopic dermatitis in a patient with Seckel syndrome.
Pediatr Dermatol. 2007 Jan-Feb; 24(1):53-6.PD

Abstract

Seckel syndrome is a very rare form of primordial dwarfism characterized by antenatal and postnatal growth delay, proportionate extreme short stature, a prominent beak-like nose, hypoplasia of the malar area, small chin, microcephaly, deformed ears lacking lobules, skeletal malformations, mental retardation, and developmental delay. This syndrome has been described with associated disorders of orthopedic, neurologic, hematologic, cardiac, and ocular systems; however, only a few reports mention dermatologic involvement. We describe a 5-year-old girl with classic Seckel syndrome who presented with moderately severe atopic dermatitis and diffuse hypopigmented macules and papules.

Authors+Show Affiliations

Texas Tech Health Sciences Center, Department of Dermatology, 3601 4th Street STOP 9400, Lubbock, TX 79430, USA.No affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article

Language

eng

PubMed ID

17300651

Citation

Brackeen, Amy, et al. "Pigmentary Changes and Atopic Dermatitis in a Patient With Seckel Syndrome." Pediatric Dermatology, vol. 24, no. 1, 2007, pp. 53-6.
Brackeen A, Babb-Tarbox M, Smith J. Pigmentary changes and atopic dermatitis in a patient with Seckel syndrome. Pediatr Dermatol. 2007;24(1):53-6.
Brackeen, A., Babb-Tarbox, M., & Smith, J. (2007). Pigmentary changes and atopic dermatitis in a patient with Seckel syndrome. Pediatric Dermatology, 24(1), 53-6.
Brackeen A, Babb-Tarbox M, Smith J. Pigmentary Changes and Atopic Dermatitis in a Patient With Seckel Syndrome. Pediatr Dermatol. 2007 Jan-Feb;24(1):53-6. PubMed PMID: 17300651.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Pigmentary changes and atopic dermatitis in a patient with Seckel syndrome. AU - Brackeen,Amy, AU - Babb-Tarbox,Michelle, AU - Smith,Jennifer, PY - 2007/2/16/pubmed PY - 2007/5/16/medline PY - 2007/2/16/entrez SP - 53 EP - 6 JF - Pediatric dermatology JO - Pediatr Dermatol VL - 24 IS - 1 N2 - Seckel syndrome is a very rare form of primordial dwarfism characterized by antenatal and postnatal growth delay, proportionate extreme short stature, a prominent beak-like nose, hypoplasia of the malar area, small chin, microcephaly, deformed ears lacking lobules, skeletal malformations, mental retardation, and developmental delay. This syndrome has been described with associated disorders of orthopedic, neurologic, hematologic, cardiac, and ocular systems; however, only a few reports mention dermatologic involvement. We describe a 5-year-old girl with classic Seckel syndrome who presented with moderately severe atopic dermatitis and diffuse hypopigmented macules and papules. SN - 0736-8046 UR - https://www.unboundmedicine.com/medline/citation/17300651/Pigmentary_changes_and_atopic_dermatitis_in_a_patient_with_Seckel_syndrome_ L2 - https://doi.org/10.1111/j.1525-1470.2007.00334.x DB - PRIME DP - Unbound Medicine ER -