Hanhart syndrome [a] is a broadly classified medical condition consisting of congenital disorders that cause an undeveloped tongue and malformed extremities and fingers. There exist five …

2020年12月21日 · Hanhart syndrome is in the group of conditions known as oromandibular-limb hypogenesis syndromes (OLHS). These syndromes are characterized by underdevelopment …

Hanhart syndrome: A rare syndrome characterized by a small jaw and tongue and absent or malformed hands and/or feet. Glossopalatine ankylosis syndrome: Children with this syndrome …

Oromandibular-limb hypogenesis syndromes (OLHS) are a group of dysmorphic complexes (including Charlie M syndrome, Hanhart syndrome and glossopalatine ankylosis; see these …

Hanhart syndrome, also known as hypoglossia-hypodactylia syndrome, aglossia-adactylia syndrome, or oromandibular limb hypogenesis syndrome, is a rare disorder of an unknown …

2022年11月26日 · Hereditary tyrosinemia type 2 or oculocutaneous tyrosinemia is also known as Richner-Hanhart syndrome. It is an autosomal recessive disorder caused by a deficiency of …

Hanhart syndrome is a rare birth defect in which the most obvious signs are a short, incompletely developed tongue (hypoglossia); absent or partially missing fingers and/or toes (hypodactylia); …

Who gets Hanhart Syndrome? (Age and Sex Distribution) Hanhart Syndrome is a rare congenital disorder. The presentation of symptoms occur at birth; Both males and females may be …

Hanhart syndrome is a rare condition that primarily affects the craniofacial region and the limbs (arms and legs). People affected by this condition are often born with a short, incompletely …

Hanhart Syndrome, also known as Hanhart Syndrome Type I and Type II, is a rare congenital disorder characterized by facial palsy and agenesis or hypoplasia of the abductor pollicis …