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1.
Rev Med Liege ; 55(8): 782-4, 2000 Aug.
Article in French | MEDLINE | ID: mdl-11051775

ABSTRACT

The "King Baby" is like a tyrant against his/her family with his/her refusing or requiring attitudes. This well known entity is analyzed in the actual social and familial context and compared with the similar situation in the countries with nutritional deficiencies. The impact of this relational problem on nutrition is detailed as especially weaning is concerned as well as the eventual consecutive and selective anorexia. A relational solution has been proposed: the "loving black-mailing" with early detection of "mothers or situations at risks".


Subject(s)
Child Behavior , Feeding Behavior , Parent-Child Relations , Social Behavior , Anorexia/etiology , Anorexia/prevention & control , Attitude , Child , Child, Preschool , Family Relations , Humans , Infant , Nutrition Disorders/etiology , Nutrition Disorders/prevention & control
2.
Am J Med Genet ; 86(5): 454-8, 1999 Oct 29.
Article in English | MEDLINE | ID: mdl-10508988

ABSTRACT

We report on a child with a generalized skin disorder associated with other minor anomalies. At birth, the child presented as a collodion baby, with patchy erythema, generalized irregular dermal atrophy, alopecia, absent eyelashes and eyebrows, and conjunctival pannus. He also had hypertelorism, prominent nasal root, large mouth, micrognathia, brachydactyly, syndactyly involving all interdigital spaces, and camptodactyly of fingers III-V. The hyperkeratotic membrane thinned progressively, leaving a mottled reticulated skin atrophy, with patchy areas of yellowish hyperpigmentation and papyraceous areas. Hair and nails were dystrophic. Mental development was borderline normal. The histological hallmarks of the skin manifestations combined orthokeratotic hyperkeratosis and marked atrophy of the dermis. The dermal extracellular matrix was immature, and factor XIII-a positive dendrocytes were rare and globular rather than dendritic. We frame as a hypothesis that the disease is due to or associated with a defect in maturation of a subset of dermal dendrocytes during fetal life. This entity may be designed as the koraxitrachitic syndrome (kappaomicronrhoalphaxi:grapnel- taurhoalphachiiotatauepsilonsigma: roughness)


Subject(s)
Abnormalities, Multiple/physiopathology , Ichthyosis, Lamellar/physiopathology , Skin Abnormalities/physiopathology , Abnormalities, Multiple/genetics , Abnormalities, Multiple/pathology , Adult , Female , Humans , Ichthyosis, Lamellar/genetics , Ichthyosis, Lamellar/pathology , Infant, Newborn , Male , Pigmentation Disorders/genetics , Pigmentation Disorders/pathology , Pigmentation Disorders/physiopathology , Skin Abnormalities/genetics , Skin Abnormalities/pathology , Syndrome
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