Trichothiodystrophy
What Is Trichothiodystrophy?
Trichothiodystrophy is a hereditary disorder characterized by brittle hair, which may be accompanied by a variety of other manifestations. It is sometimes called PIBIDS, a term that refers to the association of Photosensitivity Ichthyosis, Brittle hair, Intellectual impairment, Decreased fertility, and Short stature. Without photosensitivity the condition has been termed IBIDS, and without ichthyosis, BIDS. Many patients have recurrent infections, and abnormalities of the bone and teeth may also occur.
As more information becomes available, we will provide updates.
Longterm Course
Key Findings
- Brittle, low sulfur hair links several syndromes that may have different causes
- Skin
Fine white scale and generalized mild erythema; photosensitivity in some - Hair
Easily fractured, sparse hair - Nails
Nail plates may be abnormally thick or thin
Associated Findings
- Short stature (common)
- Central Nervous System
Intellectual impairment is usual, but of variable severity; motor development may be impaired and remain permanently deficient visual loss - Eyes
Neonatal cataracts and photophobia (common) - Genitals
Decreased fertility (common)
Resources
- Clinicians seeking to confirm a diagnosis should visit the Edvyce portal to submit a case to experts in ichthyosis.
- Learn more about FIRST’s Resources for individuals and families affected by Ichthyosis?
- Information about current clinical trials and research studies can be found here.
- Additional OMIM links: 278720, 211390, 275550, 234500
- Congenital Ichthyosiform Erythroderma (CIE)
- Lamellar Ichthyosis
- Collodion Baby
- Darier Disease
- Epidermal Nevus
- Epidermolytic Ichthyosis
- Erythrokeratodermia Variabilis
- Erythrokeratodermia Cardiomyopathy Syndrome
- Harlequin Ichthyosis
- Ichthyosis Vulgaris
- Ichthyosis with Confetti
- Keratitis-Ichthyosis-Deafness (KID)
- Netherton Syndrome
- Pachyonychia Congenita
- Palmoplantar Keratodermas
- Sjögren-Larsson Syndrome
- X-Linked Ichthyosis
- Chanarin Dorfman Syndrome
- CHILD Syndrome
- Conradi-Hünermann
- Ichthyosis Hystrix with Deafness (HID) Syndrome
- Ichthyosis Hystrix Curth-Macklin
- Refsum Disease
- Trichothiodystrophy
Phenotype Names
Trichothiodystrophy, Tay syndrome, (P)IBIDS – photosensitivity, ichthyosis, brittle hair, intellectual impairment, decreased fertility, short stature
EDD Name
KRT17-pEDD
OMIM
Inheritance
Autosomal recessive
Incidence
Rare
Diagnostic Tests
Chemical and microscopic analysis of hair; analysis of cellular DNA available for some cases.
Age of First Appearance
Birth
Abnormal Genes
transcription factors ERCC2 or ERCC3 (in some)
Primary Symptom Photos