V-shaped hyperpigmented linear lesions, patchy hypotrichosis, and teeth abnormalities in a young girl.
نویسندگان
چکیده
A 22-year-old woman presented to our Department complaining of linear hypopigmented lesions on the trunk and extremities as well as mild patchy hypotrichosis on the occipital area since infancy. Her medical history was significant for congenital dental abnormalities (hypodontiawith conical-shaped teeth) thathadbeen treated with orthodontic management and dental implants (Fig. 1). No consanguinity or similar abnormalities were recorded in the family. The patient described generalized xerosis and was aware of having hyperpigmented linear areas that were more visible after suntanning. She did not complain of reduced sweating. Physical examination revealed a fair-haired woman with scanty fine hair and an irregularly shaped occipital area of hypothrichosis. In the abnormal zone, the hair was thin and brittle with a whorly implantation (Fig. 2). Discrete eyebrow hypothrichosis was also noted. Linear hypopigmented streaks following a V-shaped pattern, intermingled with areas of normal skin, were observed on her back (Fig. 3). In addition, after a close examination, a patchy absence of vellus hair and stripes of hypotrichosis along the limbs were noted. No associated nail abnormalities were detected. A skin biopsy specimen taken from the transitional lines showed a segmental loss of eccrine sweat glands.
منابع مشابه
A Multidisciplinary Approach to a Seven Year-Old Patient with Incontinentia Pigmenti: A Case Report and Five-Year Follow Up
Incontinentia pigmenti is a rare inherited disorder involving abnormalities of the skin, hair, eyes, musculoskeletal system, central nervous system, and the teeth. Dental abnormalities are the most common manifestations of this disorder. The purpose of this case report was to present the clinical and radiological findings of a seven-year-old girl as well as the results of her five-year follow u...
متن کاملCDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
Purpose CDH3-related hypotrichosis with juvenile macular dystrophy (HJMD) is an autosomal-recessive entity characterized by congenital sparse scalp hair and macular dystrophy, leading to severe central visual loss. We report a family with HJMD caused by a novel CDH3 gene mutation and review the mutation spectrum in HJMD. A detailed phenotypic assessment for patients whose molecular results were...
متن کاملEllis-van Creveld with an Unusual Dental Anomaly: A Case Report
The Ellis-van Creveld (EVC) syndrome is a chondroectodermal dysplasia and is characterized by the cardinal features of disproportionate short stature, polydactyly, hidrotic ectodermal dysplasia, and congenital heart malformations, along with other skeletal and dental abnormalities. It is a rare condition, with very few cases reported in the medical literature. It is inherited as an autosomal re...
متن کاملA First Look: Determinants of Dental Care for Ectodermal Dysplasia Patients
Ectodermal Dysplasia (ED) is a hereditary disorder characterized by abnormal development of certain tissues and structures of ectodermal origin. The most frequently reported ED syndrome is X-linked hypohidrotic dysplasia, also known as Christ-Siemens-Touraine syndrome, which affects one to seven individuals per 10,000 live births. Orofacial characteristics of this syndrome include anodontia or ...
متن کاملHeterozygote manifestations in X-chromosomal ectodermal dysplasia
About 60-70 % of the heterozygotes of X-linked hypohidrotic ectodermal dysplasia (XLHED) show some clinical manifestations of the disease. Dental abnormalities are key diagnostic features and can be best evaluated at a young age. Compared to controls, carriers have a significantly higher frequency of agenesis of permanent teeth with persistence of deciduous teeth, small teeth resulting in gaps ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Pediatric dermatology
دوره 24 5 شماره
صفحات -
تاریخ انتشار 2007