Scarce Hair Research Articles

Trichorhinophalangeal Syndrome Type 1: Unusual Case Report and Review of Literature

Trichorhinophalangeal syndrome type 1 [TRPS1; (OMIM #190350)] is a rare autosomal dominant genetic disorder on chromosome 8q24. The carrier of the syndrome may present skeletal, craniofacial, and oral manifestations. The main characteristics that the individual may present are scarce hair or total alopecia, thin upper lip, long erased nasolabial filter, bulbous nose and low set ears. In the oral cavity, there may be changes such as supernumerary teeth and hypodontia, size changes, including macrodontia and microdontia, and teeth in malocclusion.

Novel iron oxide nanocarriers loading finasteride or dutasteride: Enhanced skin penetration for topical treatment of alopecia.

In the present study, iron oxide nanoparticles, in the form of maghemite core coated with lauric acid (ION), were synthesized and loaded with finasteride (FIN) or dutasteride (DUT) as a novel drug delivery system for the topical treatment of alopecia. Additionally, developed formulations (FIN-ION and DUT-ION) were completely elaborated with components involved in the follicle metabolism, i.e., lauric acid, which acts as a 5α-reductase inhibitor, and iron which deficiency has been related to hair loss aggravation. Stability assessment conducted over the course of 90days showed they are highly stable, with pH 7.4, constant EE% (>99%), and practically unchanged particle size and zeta potential. Besides drug distribution, the actual number of iron oxide nanoparticles, through a newly developed method using ferromagnetic resonance, was determined in each skin layer following permeation experiments. Despite the same donor concentration of colloids, nanoparticle distribution in the skin varied according to the loaded molecule. While DUT did not interfere with the nanoparticle natural tendency to accumulate within the hair follicle shafts, FIN presence hampered nanosystem interaction with the skin. Still, both formulations provided a higher skin drug penetration, compared to each respective control solution. Additionally, iron nanocarriers present a desirable visual characteristic, as the dark color aspect might instantly help disguise scarce hair follicle areas. These findings suggest the nanoformulations are highly promising for alopecia therapies.

Conventional Complete Denture in Patients with Ectodermal Dysplasia.

Ectodermal dysplasia is described as heritable conditions that involve anomalies of structures derived from the ectoderm, including hypodontia. In the cases of edentulous young patients, who did not finish their craniofacial growth, treatment with conventional complete denture is a suitable alternative. The aim of this study was to report a case of mandibular edentulism treated with conventional complete denture in a thirteen-year-old patient diagnosed with hidrotic ectodermal dysplasia. Typical features, such as frontal bossing, depressed nasal bridge, protuberant lips, scarce hair, and brittle nails, were visualized during the extraoral examination. The intraoral inspection and radiographic analysis revealed oligodontia, dental malformation, and prolonged retention of deciduous teeth at maxilla and total edentulism at mandible. A conventional complete denture was planned and constructed following the same steps of technique as recommended in adults. Although this option is not a definitive treatment, the patient and his parents were satisfied with his improvement in chewing and speech, as well as with the aesthetic benefits.

Dimorfismo sexual do gorgulho-da-goiaba Conotrachelus psidii Marshall (Coleoptera: Curculionidae)

We investigate structural and behavioral differences between male and female adults of guava weevil, Conotrachelus psidii Marshall, 1922 to help in sex determination. Weevils collected from a commercial guava orchard were individually caged and maintained under laboratory conditions. Every day ten individuals were grouped and their behavior was observed. During mating the males and females were identified. Fifty weevils of each sex were killed and they were observed with stereoscopic microscope. The antenna insertion on the rostrum and hair on the thorax and abdomen surfaces were examined. Length and width of body, pronotum, last abdominal sternite and rostrum were also taken. Behaviorally, the male weevils produce audible sound by stridulation of abdomen while females do not. In the females, the body and pronotum width and body a rostrum length were higher than in the males, but the last abdominal sternite was smaller. Three other structural differences were visible with the naked eye: 1) the anterior region of pronotum have scarce hair or have not in the females and hair is dense in the males; 2) the last tergite of females is hidden by the penultimate tergite whereas in the males is visible; 3) the first abdominal sternite of females is more prominent, very convex and without or with little bristle. In the males it is slightly concave and with abundant hair. The male-female differences found in this work allow, without hurt or change insect behavior, an efficient sex determination of guava weevil.

Síndrome de Coffin-Siris: casos clínicos y revisión de la literatura

We present the clinical cases of 2 girls, 5 and 10 years old, who presented with post natal growth retardation, mental retardation, scarce hair, body hirsutism, coarse facies, brushy eyebrows, broad nose, long filtrum, wide mouth, micrognathia, scoliosis, distal brachydactyly, prominent finger pads and hypoplastic 5th fingernails. Both patients had a normal blood cariotype, 46XX. The clinical characteristics are consistent with the diagnosis of Coffin-Siris syndrome, a genetic disorder of which there are less than 100 cases reported. Although the inheritance is apparently autosomal dominant there is still discussion about the exact mode of inheritance. The Coffin-Siris syndrome should be considered in the differential diagnosis in cases of children with mental retardation associated with coarse facies.

Metagerie - Klinisches Erscheinungsbild eines Vergreisungssyndroms

A 19-year old caucasian patient suffered from ulceration and scaring of his fingers since age two. During childhood, fibrosing contractures on the phalanges developed. Since puberty, his eunuch-like stature, bird-like face and exophthalmos had become under obvious. His hair was extraordinarily fine; his pubic hair rare. Radiological examination revealed ankylosis and osteoporosis of the phalanges and carpals. Angiography showed occlusion of multiple digital and interdigital arteries. Furthermore, a bilateral posterior cataract, restrictive respiratory disease, impaired glucose tolerance, hyperuricemia, proteinuria and primary hypogonadism were diagnosed. These findings are characteristic for the premature aging syndromes. The cardial symptoms of tall stature, bird-like face, pseudoexophthalmos, skleroderma-like and poikiloderma-like cutaneous lesions, scarce hair growth, early diabetes mellitus and arteriosclerosis led to the diagnosis of metageria.