Results 81 to 90 of about 2,045 (160)
A case of Sotos syndrome with subduroperitoneal shunt.
, 2006 The authors present a case of Sotos syndrome with increasing severity of subdural hygroma from the age of 5 months, which was managed with a subduroperitoneal shunt at 10 months of age.
Shin, YS +4 more
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Late‐Breaking Abstract Presentations
Pregnancy, Volume 2, Issue S2, September 2026.
wiley +1 more source
Сибирский научный медицинский журналThis literature review is devoted to the study of the sizes of the paranasal sinuses and nasal cavity, determined by computed tomography, depending on the shape of the skull (megacephalic, dolichocephalic, brachycephalic), gender and age.
T. A. Gridina +2 more
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KIF6 mutation in a child with intellectual disability.
, 2018 (A) A low-set prominent anti-helical left pinna. (B) MRI of the brain at 7 months-old shows dolichocephaly with a normal brain structure. (C) and (D) CT of the brain at 8 years-old, sagittal and axial views, respectively show dolichocephalic shape of the
Rungnapa Ittiwut (6008837) +11 more
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Journal of Clinical and Diagnostic ResearchIntroduction: The exploration of craniofacial relationships and their variations has historically played a significant role in differentiating racial groups within physical anthropology.
Vijay Kumar Dayma +4 more
doaj +1 more source
, 2014 Partial monosomy 8q and partial trisomy 9q due to the maternal translocation t(8;9)(q24.3;q34.1): a case report: Partial trisomy 9q34-qter and partial monosomy 8q24.3-qter are very rare chromosomal abnormalities.
Ikbal, MEVLİT +4 more
core
Maguaré, 2005 En el lote ubicado en la Cra. 5 Nº 2-41 de Madrid, Cundinamarca, se rescató un yacimiento arqueológico consistente en un montículo funerario y un conjunto ceremonial.
José Vicente Rodríguez +1 more
doaj +2 more sources
A Novel NPR2 Mutation in Two Turkish Siblings with Acromesomelic Dysplasia Maroteaux Type
, 2020 Acromesomelic Dysplasia Maroteaux type (AMDM) which belongs to the group of acromesomelic dysplasias is an extremely rare skeletal disorder described by severe shortening of the forelimbs and disproportionate short stature. AMDM is an autosomal recessive
Adanur, Kübra +5 more
core
, 2006 BACKGROUND: Pfeiffer syndrome (PS; OMIM #101600) is an autosomal dominant disorder characterized by craniosynostosis, midface hypoplasia, broad thumbs, brachydactyly, broad great toes, and variable syndactyly.
Fanganiello, Roberto D. +3 more
core +1 more source
Maguaré, 2009 En el lote ubicado en la Cra. 5 Nº 2-41 de Madrid, Cundinamarca, se rescató un yacimiento arqueológico consistente en un montículo funerario y un conjunto ceremonial.
José Vicente Rodríguez +1 more
doaj