agenosomia


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Related to agenosomia: anosmia

anomaly

 [ah-nom´ah-le]
marked deviation from normal. adj., adj anom´alous.
Axenfeld's anomaly a developmental anomaly characterized by a circular opacity of the posterior peripheral cornea, and caused by an irregularly thickened, axially displaced Schwalbe's ring.
congenital anomaly (developmental anomaly) absence, deformity, or excess of body parts as the result of faulty development of the embryo.
Ebstein's anomaly see ebstein's anomaly.
May-Hegglin anomaly a rare dominantly inherited disorder of blood cell morphology, characterized by RNA-containing cytoplasmic inclusions (similar to Döhle bodies) in granulocytes, by large, poorly granulated platelets, and by thrombocytopenia.

a·gen·o·so·mi·a

(ā-gen-ō-sō'mē-ă),
Markedly defective formation or absence of the genitalia; usually accompanied by protrusion of the abdominal viscera through an incomplete abdominal wall.
[G. a- priv. + genos, sex, + soma, body]

agenosomia

/ageno·so·mia/ (ah-jen″ah-so´me-ah) congenital absence or imperfect development of the genitals and eventration of the lower part of the abdomen.

agenosomia

[əjen′əsō′mē·ə]
a congenital malformation characterized by the absence or defective formation of the genitals and protrusion of the intestines through an incompletely developed abdominal wall.

Agenosomia

A virtually extinct nonspecific term for distorted or rudimentary development of the external genitalia.

a·gen·o·so·mi·a

(ā'jen-ō-sō'mē-ă)
Markedly defective formation or absence of the genitalia; usually accompanied by protrusion of the abdominal viscera through an incomplete abdominal wall.
[G. a- priv. + genos, sex, + soma, body]

agenosomia

imperfect development of reproductive organs.
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