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Long narrow head

Known as: DOLICHOCEPHALY, Dolicocephaly, Large dolichocephalic skull 
An abnormality of skull shape characterized by a increased anterior-posterior diameter, i.e., an increased antero-posterior dimension of the skull… 
National Institutes of Health

Related topics

Related topics

40 relations
22q13.3 Deletion SyndromeAU-KLINE SYNDROMEBloom SyndromeCRANIOECTODERMAL DYSPLASIA 2

Narrower (1)

Scaphycephaly

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2005
2005
Calcium and phosphorus nutrition in preterm infants.
Metabolic bone disease is a common event in preterm infants. Between 24 wk gestation and term, the fetus accrues approximately 80… 
Review
2000
Review
2000
Ring chromosome 22 and autism: report and review.
Ring chromosome 22 has been described in over 50 cases. A characteristic phenotype has not been fully delineated; however, long… 
Highly Cited
1998
Highly Cited
1998
The differential diagnosis of abnormal head shapes: separating craniosynostosis from positional deformities and normal variants.
The correct differential diagnosis of an abnormal head shape in an infant or a child is vital to the management of this common… 
Review
1997
Review
1997
Expanded phenotype of cranioectodermal dysplasia (Sensenbrenner syndrome)
Cranioectodermal dysplasia (CED) is an autosomal recessive condition characterized by defects of ectoderm-derived structures and… 
Review
1996
Review
1996
Odontodysplasia, gingival manifestations, and accompanying abnormalities.
1995
1995
Skull morphology affected by different sleep positions in infancy.
In infancy, prior to cranial suture and fontanel calcification, the craniofacial skeleton can be easily deformed by an externally… 
Review
1989
Review
1989
Emerging phenotype of duplication (7p): a report of three cases and review of the literature.
Here we report on three patients with dup (7p) and review the previously published 17 cases. Characteristic manifestations… 
1978
1978
Partial trisomy of the short arm of chromosome 7 due to a familial translocation rcp(7;14) (p11;p11)
A boy with trisomy of the short arm of chromosome 7 is reported. He presented several congenital malformations, such as… 
1975
1975
Partial trisomy 9q: A new syndrome
SummaryTwo unrelated patients with a strikingly similar phenotype (low birth weight and poor thriving; mental retardation… 
1957
1957
Marfan's syndrome: description of a family.
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