Neonatal Erythroderma: Diagnostic Challenges and the Limitations of Genetic Testing. [PDF]
Phipps J, Popescu O.
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A Case Of Harlequin Fetus With Psoriasis In His Family
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Diagnostic Concordance and Interobserver Variability Between Tele-Dermatology (Store-and-Forward) and In-Person Evaluation for Inpatient Dermatology Consultations. [PDF]
Gupta P, Pandhi D, Grover C, Kumar R.
europepmc +1 more source
Combined Complementary and Alternative Therapies for the Management of a Breech Fetus: A Feasibility Study. [PDF]
Babbar S, Williams KB, Vawter L.
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Harlequin fetus with polydactyly and renal dysplasia.
S, Vijayaragavan +4 more
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Potential of 3D Skin Models and N/TERT-2G Cell Line in Genetic Research on Autosomal Recessive Nonsyndromic Epidermal Differentiation Disorders. [PDF]
Hsu-Rehder HH +9 more
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Dental Abnormalities in Congenital Ichthyoses: Case Report and Review of the Literature. [PDF]
Maarouf S, Clark M, Chen A, Haggstrom A.
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Related searches:
Harlequin fetus and micromelia
Prenatal Diagnosis, 1989AbstractA fetus was born prematurely after a 34‐week pregnancy whose evolution was marked by the ultrasonic finding at 23 weeks of a considerable shortening of the long bones. At birth, the newborn infant bore the appearance of a harlequin fetus.
A, Charles, R, Moulinasse, L, Versailles
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Harlequin fetus: a case report
Surgical and Radiologic Anatomy, 1999We report a case of harlequin fetus. This very rare cutaneous malformation is a severe form of congenital ichthyosis. This disorder is due to an inborn error of epidermal keratinization. Malformations of ears, nose, and hypoplasia of fingers or nails are seen. This affection is most often lethal.
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