Search results
Results From The WOW.Com Content Network
Leontiasis ossea, also known as leontiasis, lion face or lion face syndrome, is a rare medical condition, characterized by an overgrowth of the facial and cranial bones. It is not a disease in itself, but a symptom of other diseases, including Paget's disease, fibrous dysplasia, hyperparathyroidism and renal osteodystrophy. [citation needed]
Leonine facies is a facies that resembles that of a lion. It is seen in multiple conditions and has been classically described for lepromatous leprosy as well as Paget's disease of bone. It is a dermatological symptom, with characteristic facial features that are visible on presentation, and is useful for focusing on differential diagnosis.
Pitt–Hopkins syndrome; Beta thalassemia is associated with distinctive facial features due to ineffective erythropoiesis. The ineffective erythropoiesis causes marrow hyperplasia or expansion and bony changes, including the bones of the face; this causes craniofacial protrusions. [5] Mowat–Wilson syndrome; Snijders Blok–Campeau syndrome ...
Craniodiaphyseal dysplasia (CDD), also known as lionitis, is an extremely rare autosomal recessive bone disorder that causes calcium to build up in the skull, disfiguring the facial features and reducing life expectancy.
In 1978 Azusa, California, Rocky Dennis, a teenage boy with the extremely rare genetic disorder known as craniodiaphyseal dysplasia, is accepted without question by his freewheeling biker mother's boyfriend Gar, who is a father figure to him, his "extended motorcycle family," and his maternal grandparents who share his passion of baseball card collecting; but is treated with fear, pity ...
A Tennessee man has a rare disorder that causes faces to appear distorted in shape, size, texture or color. To him, images show, they look demonic. ... to modify the pictures to match Sharrah’s ...
Get AOL Mail for FREE! Manage your email like never before with travel, photo & document views. Personalize your inbox with themes & tabs. You've Got Mail!
Pfeiffer syndrome is a rare genetic disorder, characterized by the premature fusion of certain bones of the skull (craniosynostosis), which affects the shape of the head and face. The syndrome includes abnormalities of the hands and feet, such as wide and deviated thumbs and big toes.