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Frontal bossing
Known as:
Frontal protruberance
, Skull bossing
A skeletal deformity characterized by an unusually prominent forehead. Causes include acromegaly, Hurler syndrome, Silver-Russell syndrome, and…
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National Institutes of Health
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Related topics
Related topics
50 relations
AMINOPTERIN SYNDROME SINE AMINOPTERIN
Achondroplasia
Achondroplasia, Severe, With Developmental Delay And Acanthosis Nigricans
Atelosteogenesis Type 3
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
A CASE OF HURLER SCHEIE SYNDROME, ATTENUATED FORM OF MUCOPOLYSACCHARIDOSIS TYPE I -
M. Sinharay
,
Mousumi Mukhopadhyay
2013
Corpus ID: 58730406
Mucopolysaccharidosis type Ι or MPS Ι is an autosomal recessive inborn error of metabolism due to deficiency of α-L-iduronidase…
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2010
2010
Cleidocranial dysplasia: a dilemma in diagnosis?
Pradhuman Verma
,
K. Verma
,
S. Gupta
2010
Corpus ID: 26423765
Abstract Cleidocranial dysplasia is a developmental anomaly and is characterized by craniofacial and skeletal malformations as…
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2009
2009
Remodelación craneal para craneosinostosis sagital mediante osteotomía en forma de espiral usando sistema de fijación con miniplacas y tornillos absorbibles
Oscar Solís-Salgado
,
M. Anaya-Jara
2009
Corpus ID: 74240235
Sagittal synostosis is the most common craniosynostosis. Sagittal synostosis is identified by the characteristic dolichocephaly…
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Review
2009
Review
2009
An investigation of sociability : delineating a behavioural and social phenotype for Monosomy 1p36 Deletion Syndrome.
F. Cook
2009
Corpus ID: 141286881
There is a substantial body of research indicating that compromised social functioning for individual with intellectual…
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2000
2000
Achondroplasia and nail-patella syndrome: the compound phenotype
M. J. Wright
,
M. Ain
,
M. Clough
,
G. Bellus
,
O. Hurko
,
I. Mcintosh
Journal of Medical Genetics
2000
Corpus ID: 13631127
Editor—Achondroplasia (MIM 100800) is one of the most common chondrodysplasias with a prevalence rate of around 1 in 26 000 live…
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1999
1999
Molecular analysis of a translocation (6;11)(p21;q25) in a girl with Jacobsen syndrome.
Cora M. Aalfs
,
J. Hoovers
,
F. Wijburg
American journal of medical genetics
1999
Corpus ID: 24097020
More than 70 patients with Jacobsen syndrome have been described [Penny et al., 1995; Pivnick et al., 1996; Ono et al., 1996…
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Review
1992
Review
1992
Delayed membranous cranial ossification in a mother and child.
A. G. Angel
,
A. Carnevale
,
R. Takenaga
American journal of medical genetics
1992
Corpus ID: 7054352
We report on a girl and her mother with delayed intramembranous ossification of the cranial vault. The 11-month-old girl had a…
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1987
1987
Soft-tissue frontal bossing.
B. Guyuron
Plastic and Reconstructive Surgery
1987
Corpus ID: 34771191
An unusual case of frontal bossing due to excess subcutaneous fibroadipose tissue in a 38-year-old woman with Möbius syndrome is…
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1984
1984
FG syndrome in a premature male.
D. Bianchi
American journal of medical genetics
1984
Corpus ID: 22490235
A 30-week premature male infant is presented with dolichocephaly, frontal bossing, down-slanting palpebral fissures…
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1982
1982
Two chromosomal syndromes in the same family: Monosomy and trisomy for part of the short arm of chromosome 10
S. Slinde
,
I. Hansteen
European Journal of Pediatrics
1982
Corpus ID: 39052413
A grandfather with balanced translocation t(1∶10) gave rise to three possible combinations involving chromosome 10: balanced…
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