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Hanhart's syndrome
Known as:
Hanhart syndrome
, Oromandibular limb hypogenesis complex
National Institutes of Health
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Related topics
Related topics
3 relations
Broader (3)
Craniofacial Abnormalities
Limb Deformities, Congenital
Multiple congenital anomalies
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2019
Review
2019
HANHART SYNDROME: A RARE CASE REPORT AND REVIEW OF LITERATURE
Shreya Das
,
Anjana Mazumdar
,
B. Maity
,
S. Ghose
Indian Journal of Case Reports
2019
Corpus ID: 87513209
Hanhart syndrome is a rare congenital and genetic disease, in which the most common signs are short, incompletely developed…
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2019
2019
Hanhart syndrome: hypoglossia-hypodactylia syndrome
I. Varal
,
P. Doğan
The Pan African Medical Journal
2019
Corpus ID: 196529813
Hanhart syndrome is a congenital disorder that causes an undeveloped tongue and malformed extremities and fingers. Small mouth…
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2016
2016
A Rare Case of Hanhart Syndrome with Mild Developmental Delay.
G. Gulec Ceylan
,
T. Tos
,
E. Sari
Genetic Counseling
2016
Corpus ID: 3639706
Hanhart Syndrome (OMIM 103300) is an extremely rare syndrome with some congenital malformations. It is characterized by…
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2013
2013
Síndrome de Hanhart: caso clínico
Helena Rios
,
Cátia Carnide
,
+4 authors
L. Ramos
2013
Corpus ID: 73409132
Introduction: In 1950, Hanhart described three cases of aglossia and limb malformations. The association of congenital…
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2011
2011
Case Report: Prosthetic Fitting of Patient With Bilateral Peromelia of Lower and Upper Limbs Secondary to Hanhart Syndrome
B. Harder
,
C. Ferraro
2011
Corpus ID: 75969259
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…
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2010
2010
Hanhart syndrome.
D. Dogan
,
M. Dŏgan
,
M. Aslan
,
E. Menekşe
,
C. Yakinci
Genetic Counseling
2010
Corpus ID: 25613212
We report on a male infant with Hanhart Syndrome. It is classified in "oromandibular limb hypogenesis syndromes" which are a…
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2007
2007
Increased frequency of severe major anomalies in children conceived by intracytoplasmic sperm injection
I. Sánchez-Albisua
,
S. Borell-Kost
,
U. Mau-Holzmann
,
P. Licht
,
I. Krägeloh-Mann
Developmental Medicine & Child Neurology
2007
Corpus ID: 42076594
The neurodevelopmental outcome of children born after intracytoplasmic sperm injection (ICSI) is controversial. We compared the…
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1982
1982
Limb deficiency and splenogonadal fusion.
R. Pauli
,
A. Greenlaw
American journal of medical genetics
1982
Corpus ID: 20875874
We report a 10-year-old boy with tetramelic limb deficiencies, splenogonadal fusion, and mild mandibular and oral abnormalities…
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1982
1982
Hanhart syndrome: possibility of autosomal recessive inheritance.
H. Dellagrammaticas
,
M. Tzaki
,
+4 authors
C. Bartsocas
Progress in clinical and biological research
1982
Corpus ID: 32934000
Review
1976
Review
1976
Studies of malformation syndromes of man XXXXI B: Nosologic studies in the Hanhart and the Möbius syndrome
J. Herrmann
,
Pallister Pd
,
+4 authors
J. Opitz
European Journal of Pediatrics
1976
Corpus ID: 23498856
We reviewed etiologic and phenotypic aspects of those orofacial and limb anomalies usually diagnosed as Hanhart syndrome and M…
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