What is Charlie syndrome?
Charles Bonnet syndrome causes a person whose vision has started to deteriorate to see things that aren’t real (hallucinations). The hallucinations may be simple patterns, or detailed images of events, people or places.
Who has Hanhart syndrome?
Hanhart syndrome is a very rare developmental disorder that affects males and females in equal numbers. Fewer than 1 in 20,000 children are affected with this disorder. Approximately 30 cases of Hanhart syndrome were reported in the medical literature from 1932 to 1991.
What is Kindler syndrome?
Kindler syndrome is a rare type of epidermolysis bullosa, which is a group of genetic conditions that cause the skin to be very fragile and to blister easily. From early infancy, people with Kindler syndrome have skin blistering, particularly on the backs of the hands and the tops of the feet.
What is Liddle syndrome?
Description. Collapse Section. Liddle syndrome is an inherited form of high blood pressure (hypertension). This condition is characterized by severe hypertension that begins unusually early in life, often in childhood, although some affected individuals are not diagnosed until adulthood.
Is Hanhart syndrome genetic?
The exact underlying cause of Hanhart syndrome is currently unknown. However, researchers suspect that there may be genetic and/or environmental factors that contribute to the development of the condition.
Could Jacobsen syndrome have been prevented?
There is no cure for Jacobsen syndrome ; treatment generally focuses on the specific signs and symptoms present in each individual. Treatment may require the coordinated efforts of a team of various specialists. Individuals with low platelet counts ( thrombocytopenia ) should be monitored regularly.
What is a person without legs called?
(legləs ) 1. adjective [ADJECTIVE noun] A legless person or animal has no legs.
What is Hypoglossia-hypodactyly syndrome (OMIM 103300)?
Discussion. Hypoglossia-hypodactyly syndrome (OMIM 103300) is a rare syndrome which was classified by Hall as ‘oromandicular and limb hypogenesis syndrome’ (OLHS). OLHS is characterized by a hypoplastic mandible, absence of the lower incisors, hypoglossia, abnormalities of digits and limbs which range from syndactyly to amelia [ 1 ].
What is Aglossia-adactyly syndrome?
Aglossia-adactyly syndrome (Concept Id: C1863203) Hypoglossia-hypodactyly syndrome is characterized by a hypoplastic mandible, absence of the lower incisors, hypoglossia, and a variable degree of absence of the digits and limbs. Intelligence is normal (Hall, 1971).
What is oromandibular limb hypogenesis syndrome?
The Oromandibular Limb Hypogenesis Syndromes (OLHS) comprises a spectrum of disorders involving the tongue, mandible, and the limbs and are characterized by hypoplastic mandible, absence of the lower incisors, hypoglossia, digits and limbs abnormalities ranges from syndactyly to amelia.