Hereditary hypotrichosis simplex of the scalp: A case report with 10 affected members in a family
Journal Title: Indian Journal of Case Reports - Year 2018, Vol 4, Issue 4
Abstract
Hereditary hypotrichosis simplex of the scalp is an autosomal dominant disorder, characterized by sparse or absent scalp hairs without structural defects, in the absence of other ectodermal or systemic abnormalities. Hairs are usually normal at birth but thin progressively during childhood to become very sparse or may be absent by the third decade. Hair loss is confined only to the scalp with normal growth of facial and body hairs.
Authors and Affiliations
Anuradha K. Babu, Jyoti Bai S
Management of temporomandibular joint dislocations in the emergency department - a case series
The temporomandibular joint (TMJ) or TMJ is a type of ginglymoarthrodial joint and its articulation involves both sliding and hinge type movements. Dislocation of this joint is a very painful condition and needs acute em...
Unilateral reexpansion pulmonary edema after tube thoracostomy: A case report
We report a case of unilateral reexpansion pulmonary edema (RPE) in a patient of secondary spontaneous pneumothorax of 2 days’ duration developed after tube thoracostomy. RPE is an unusual but life-threatening complicati...
An unusual presentation of anterior urethral valve in a child with diabetes mellitus
Anterior urethral valve (AUV) is identified to be a common source of congenital obstructive lesion of the anterior urethra. Up to 80% of children with AUVs develop bladder dysfunction, bladder instability, hyperreflexia,...
Basal Cell Adenoma: A rare case report with immunohistochemical analysis
Basal cell adenoma (BCA) of the salivary gland is a rare benign monomorphic adenoma accounting for approximately 1–2% of all salivary gland tumors. It is characterized by the presence of sheets/nests of monomorphic cells...
Poland syndrome with some rare associations, and brief literature review
Poland syndrome (PS) is a rare congenital condition with predominant unilateral chest wall deformity due to hypoplasia of the pectoralis muscles. However, its clinical features are highly variable as all the features may...