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Table 2 Medical history

From: No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia

Code

Diseases other than XLHED

Recurrent eye problems

Hearing impairment

Photophobia

Conjunctivitis

F1_S1

Allergy

N

N

N

F1_S2

NAD

N

N

N

F1_M

NAD

N

N

N

F2_S1

Urticaria, neurodermatitis

Y

Y

Y

F2_S2

NAD

Y

N

N

F2_M

NAD

Y

N

N

F3_S1

Diabetes

Y

N

Y

F3_S2

NAD

Y

N

N

F4_S1

NAD

N

N

N

F4_S2

Hashimoto's thyroiditis

N

Y

N

F4_M

Hypothyroidism

N

Y

N

F5_S1

Glaucoma

Y

N

N

F5_S2

Hypothyroidism

N

N

N

F6_S1

Hypothyroidism

N

N

N

F6_S2

Allergy, eczema

N

N

N

F6_M

NAD

N

N

N

  1. Abbreviations: F, family; S, sister; M, mother; NAD, no abnormality detected; Y, yes; N, no
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Orphanet Journal of Rare Diseases

ISSN: 1750-1172