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Hanhart's syndrome

Known as: Hanhart syndrome, Oromandibular limb hypogenesis complex 
National Institutes of Health

Papers overview

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Review
2019
Review
2019
Hanhart syndrome is a rare congenital and genetic disease, in which the most common signs are short, incompletely developed… 
2019
2019
Hanhart syndrome is a congenital disorder that causes an undeveloped tongue and malformed extremities and fingers. Small mouth… 
2016
2016
Hanhart Syndrome (OMIM 103300) is an extremely rare syndrome with some congenital malformations. It is characterized by… 
2013
2013
Introduction: In 1950, Hanhart described three cases of aglossia and limb malformations. The association of congenital… 
2011
2011
A 14-year-old man presented with peromelia of all four limbs secondary to Hanhart syndrome. The lower limbs were 11 cm and 12 cm… 
2010
2010
We report on a male infant with Hanhart Syndrome. It is classified in "oromandibular limb hypogenesis syndromes" which are a… 
2007
2007
The neurodevelopmental outcome of children born after intracytoplasmic sperm injection (ICSI) is controversial. We compared the… 
1982
1982
We report a 10-year-old boy with tetramelic limb deficiencies, splenogonadal fusion, and mild mandibular and oral abnormalities… 
Review
1976
Review
1976
We reviewed etiologic and phenotypic aspects of those orofacial and limb anomalies usually diagnosed as Hanhart syndrome and M…