Wolf-Hirschhorn syndrome - Medtick

Wolf-Hirschhorn syndrome

What is it?

Wolf-Hirschhorn syndrome is a rare chromosomal disorder/ginetic disorder that can lead to birth defects and developmental problems.

  • The symptoms of this syndrome vary from person to person based the size and location of the missing piece of chromosome 4.
  • Disorder occurred in approximately 1 in about 50,000 live births with a female to male ratio of 2:1.
  • In most cases, this is not an inherited genetic disorder but rather a mutation that occurs spontaneously (90%).
  • 10% chance it can be inherited

National Organization for Rare Disorders. Wolf-Hirschorn syndrome. Updated 2017.

Cause

  • Missing piece (partial deletion or monosomy) of the short arm of chromosome 4.
  • Chromosomes are found in the nucleus of all body cells.
  • They carry the genetic characteristics of each individual. Pairs of human chromosomes are numbered from 1 through 22, with the 23rd pair made up of the X and Y chromosomes, with XX associated with female sex, and XY associated with male sex. Each chromosome has a short arm designated “p” and a long arm designated “q.” Chromosomes are further sub-divided into numbered bands.
  • For example, “chromosome 4p16.3” (pronounced “four p one-six point three”) refers to band 16.3 on the short arm of chromosome 4. The numbered bands are used to specify the location of the genes found on each chromosome.
  • Deletion of part of the short arm of chromosome 4 (4p) causes this disorder. It is believed that a portion of band 16.3 on chromosome 4p (4p16.3) is the “critical region” for the disorder, meaning that deletion of this area leads to full expression of Wolf-Hirschhorn syndrome.
  • In most people, the deletion causing WHS happened extremely early in that individual’s development (possibly in the egg or sperm prior to fertilization) and is not inherited from that person’s parents (this is referred to as spontaneous or de novo). Much less commonly, the disorder is inherited from a parent who has a balanced translocation.
  • A translocation is an abnormal chromosome made when pieces of two or more chromosomes break off and trade places. If all of the parts of both chromosomes that participated in the swap are present, this is said to be “balanced.” Because a person with a balanced translocation has all the necessary genetic material for normal development, individuals with balanced translocations do not usually have health problems related to their abnormal chromosome.
  • Unfortunately, a balanced translocation can be transmitted to a child in an unbalanced fashion, leading to missing or extra genetic material in a child and causing a chromosome disorder like WHS.
  • Chromosome (cytogenetic) testing can determine if a parent has a balanced translocation.

National Organization for Rare Disorders. Wolf-Hirschorn syndrome. Updated 2017.

Symptoms

(Symptoms can vary from individual to individual)

  • Small head (microcephaly)?
  • Arched eyebrows?
  • Wide-set eyes (ocular hypertelorism)?
  • Eye differences (turning in or out of the eyes, eye malformations)?
  • Droopy eyelids?
  • Ear differences (small, simple, tags and/or pits)?
  • Low-set malformed ears?
  • Broad or beaked nose?
  • Cleft lip and/or high arched palate (roof of the mouth)?
  • Thin upper lip /Short upper lip?
  • Small jaw  and/or small mouth  and/or Small lower part of the face?
  • Problems with teeth?
  • Feeding problems/swallowing difficulties?
  • Slowed growth and/or shorter than average?
  • Heart (cardiac) defects/atrial septal defect (‘hole in the heart’):
    • Short of breath and/or breathing difficulties (whether after exercise or not) and/or wheezing?
    • Regular and reoccurring chest infections?
    • Heart palpitations and/or irregular heartbeats?
  • Difficult to concentrate /difficulty in concentrating/memory problems and/or learning difficulties?
  • Abnormalities of the kidneys/Pain in pelvis area and/or lower back and/or intense pain in the back or side (or moving pain from back to side) or in groin area?
  • Incontinence?
  • Abnormalities of the penis (opening of penis in wrong place), testicles (failure of testicles to fall to right position), or vagina (Blockage of the vagina)/Underdevelopment or malformation of genitals and urinary tract?
  • Problems with bones?
  • Malformation of the hands, feet, chest, and spine?
  • Low muscle tone and poor muscle development/ Loss of muscle and/or muscle are shrinking?
  • Bone and joint movement problems and/or difficulty using arms and/or body and/or legs and/or lack of stamina and/or walking difficulties and/or crawling difficulties and/or rolling over difficulties?
  • Creases across the palms called ‘simian creases’?
  • Seizures?

Complications /Information to beware of/General tips:

Medical Emergency Condition

And/or do not wait, phone for an ambulance if have or develop:


This condition may show similar symptoms to:

NORD


These conditions are very difficult to diagnose, a specialist opinion is required.

OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. While the OMIM database is open to the public, users seeking information about a personal medical or genetic condition are urged to consult with a qualified physician for diagnosis and for answers to personal questions.

Detailed Information

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