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Hypoglossia-hypodactyly syndrome
rareA 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 developed tongue; absent or partially missing fingers and/or toes; abnormalities of the arms and/or legs; and an extremely small jaw. The severity of these physical abnormalities varies greatly among affected people, and children with this condition often have some, but not all, of the symptoms. The cause of Hanhart syndrome is not fully understood. Treatment depends on the signs and symptoms present in each person.
- Identifiers
- MONDO:0007073 OMIM:103300Orphanet:989
- Part of
- Congenital limb malformationMultiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndromeNon-syndromic limb reduction defectOromandibular-limb hypogenesis syndrome
- Also known as
- aglossia adactylia · aglossia-adactylia syndrome · Hanhart Syndrome · Hypoglossia-hypodactylia syndrome · Jussieu syndrome
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