WordNet

part of an insects body that bears the wings and legs
the part of the human torso between the neck and the diaphragm or the corresponding part in other vertebrates (同)chest, pectus
the middle region of the body of an arthropod between the head and the abdomen
an affliction in which some part of the body is misshapen or malformed (同)malformation, misshapenness

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1. 漏斗胸 pectus carinatum
2. 再発性多発性軟骨炎の診断的評価 diagnostic evaluation of relapsing polychondritis
3. 骨軟化症の臨床症状、診断、および治療 clinical manifestations diagnosis and treatment of osteomalacia
4. 外反母趾変形（バニオン） hallux valgus deformity bunion
5. 気管の放射線学 radiology of the trachea

Fibrodysplasia ossificans progressiva: initial presentation with a preosseous lesion of the scalp and its MRI appearance.

Lin FY1, Lin CH1, Shu G1, Chen CK2,3.
Skeletal radiology.Skeletal Radiol.2016 Jul;45(7):991-6. doi: 10.1007/s00256-016-2359-x. Epub 2016 Mar 22.
This case subject is a 1-year-old girl presenting with recurrent diffuse soft-tissue swelling of the scalp and periorbital region. Her family denied any known history of trauma. There was no obvious discoloration or local heat at the lesion. Magnetic resonance imaging (MRI) revealed diffuse soft tis
PMID 27003387

Transplacental sildenafil rescues lung abnormalities in the rabbit model of diaphragmatic hernia.

Russo FM1, Toelen J2, Eastwood MP3, Jimenez J4, Miyague AH3, Vande Velde G5, DeKoninck P3, Himmelreich U6, Vergani P7, Allegaert K8, Deprest J9.
Thorax.Thorax.2016 Jun;71(6):517-25. doi: 10.1136/thoraxjnl-2015-207949. Epub 2016 Mar 17.
INTRODUCTION: The management of congenital diaphragmatic hernia (DH) would benefit from an antenatal medical therapy, which addresses both lung hypoplasia and persistent pulmonary hypertension. We aimed at evaluating the pulmonary effects of sildenafil in the fetal rabbit model for DH.METHODS: We pe
PMID 26987998

Maladaptative autophagy impairs adipose function in Congenital Generalized Lipodystrophy due to cavin-1 deficiency.

Salle-Teyssières L1, Auclair M1, Terro F1, Nemani M1, Elsayed SM1, Elsobky E1, Lathrop M1, Délépine M1, Lascols O1, Capeau J1, Magré J1, Vigouroux C1.
The Journal of clinical endocrinology and metabolism.J Clin Endocrinol Metab.2016 May 4:jc20161086. [Epub ahead of print]
CONTEXT: Mutations in PTRF encoding cavin-1 are responsible for congenital generalized lipodystrophy type 4 (CGL4) characterized by lipoatrophy, insulin resistance, dyslipidemia and muscular dystrophy. Cavin-1 cooperates with caveolins to form the plasma membrane caveolae, involved in cellular traff
PMID 27144934

Relationship between the Degree of Thoracic Deformity and the Angle Formed by a Line Connecting the Sternum and the Spinous Process of the Vertebrae in Individuals with Severe Motor and Intellectual Disorders