The non-syndromic anterior cervical hypertrichosis (OMIM N° 600457) is a genetic disorder characterized by a patch of hair at the level of the laryngeal prominence. We present a 12-year-old boy with anterior cervical hypertrichosis and mild generalized hypertrichosis. He has no neurological, ophthalmological or skeletal anomalies. The clinical follow up is 10 years.
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http://dx.doi.org/10.5546/aap.2016.e314 | DOI Listing |
Dermatol Surg
December 2024
UnionDerm, New York, New York.
Background: Adult populations have traditionally been the primary recipients of cosmetic treatments, but a growing trend shows an increase in such procedures among pediatric patients.
Objective: The objective of the authors' study was to investigate types of procedures currently being performed by pediatric and cosmetic dermatologists and factors that may influence their choice of treatments in a pediatric population.
Methods: The authors conducted an anonymous online survey targeting healthcare practitioners who frequently use lasers for pediatric cutaneous conditions.
Indian J Otolaryngol Head Neck Surg
June 2024
Department of Otorhinolaryngology and Head & Neck Surgery, Apollo Hospital International Limited, Gandhinagar, Gujarat India.
Unlabelled: A case of congenital hemifacial hypertrophy is described. This rare condition is more prevalent in males, and it is characterized by facial asymmetry. Sometimes, Hemifacial hypertrophy can lead to obstruction of the respiratory airway which may prove lethal.
View Article and Find Full Text PDFCoffin-Siris syndrome (CSS) is a rare autosomal dominant inheritance disorder characterized by distinctive facial features, hypoplasia of the distal phalanx or nail of the fifth and additional digits, developmental or cognitive delay of varying degree, hypotonia, hirsutism/hypertrichosis, sparse scalp hair and varying kind of congenital anomalies. CSS can easily be misdiagnosed as other syndromes or disorders with a similar clinical picture because of their genetic and phenotypic heterogeneity. We describde the genotype-phenotype correlation of one patient from a healthy Chinese family with a novel genotype underlying CSS, who was first diagnosed in the ophthalmology department as early-onset high myopia (eoHM).
View Article and Find Full Text PDFPediatr Dermatol
July 2024
Pennsylvania State College of Medicine, Hershey, Pennsylvania, USA.
Diffuse neurofibroma is a rare type of neurofibroma uncommonly reported in infancy. It is a slow growing tumor originating in the peripheral nerve sheath. We present the case of a 17-month-old boy with diffuse neurofibroma of the scalp associated with hypertrichosis.
View Article and Find Full Text PDFIndian J Dermatol Venereol Leprol
January 2024
Department of Dermatology, Venereology and Leprosy, Institute of Naval Medicine, INHS Asvini, Colaba, Mumbai, Maharashtra, India.
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